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Neonatal neurology
Author:
ISBN: 9780702036088 0702036080 9780443067242 0443067244 Year: 2007 Publisher: [Place of publication not identified] Churchill Livingstone Elsevier

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Abstract

Completely updated, thoroughly referenced, and well illustrated, the fourth edition of Gerald Fenichel's classic review, Neonatal Neurology walks you through the latest advances in the clinical diagnosis and management of neurological disorders in the newborn.


Periodical
Donald School journal of ultrasound in obstetrics and gynecology.
Author:
ISSN: 09751912 Year: 2007 Publisher: New Delhi : Jaypee Bros. Medical Publishers


Book
Atopic eczema in children : management of atopic eczema in children from birth up to the age of 12 years
Authors: ---
ISBN: 190475242X Year: 2007 Publisher: [Place of publication not identified] RCOG Press

Smith's recognizable patterns of human deformation
Authors: ---
ISBN: 9781437713138 1437713130 9780721614892 0721614892 Year: 2007 Publisher: [Place of publication not identified] Saunders/Elsevier


Book
Hereditary nonpolyposis colorectal cancer : diagnostic strategies and their implications
Authors: --- ---
ISBN: 1587632489 Year: 2007 Publisher: [Place of publication not identified] U S Dept of Health and Human Services Public Health Service Agency for Healthcare Research and Q

Fetal and Neonatal Pathology
Authors: ---
ISBN: 9781846287435 1846285240 9781846285240 9786612930898 1282930893 184628743X Year: 2007 Publisher: London : Springer London : Imprint: Springer,

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Abstract

Fetal and Neonatal Pathology is the Fourth Edition of what has become the classic reference in the field of fetal and neonatal pathology. Fully revised and up-dated, the book retains the overall format of previous editions, presenting the same practical approach to the examination of both fetuses and perinatal deaths. It provides essential clinical and pathophysiological information and discusses the pathogenesis of abnormalities as a basis for appropriate methods of investigation. Part 1 deals with the examination of the products of conception after the termination of pregnancy for fetal anomalies. The range of pathological abnormalities is described and their relevance discussed. Special attention is paid to the differences in pathological findings of specific conditions between the second and third trimesters. Part 2 is organised by system, describing and illustrating those pathological problems which are likely to be encountered in the fetus and neonate. Each chapter is introduced by a concise account of the development of the relevant system. There is also a discussion, as appropriate, of changes at birth as well as changes in normal function that may occur during the neonatal period. Fetal and Neonatal Pathology, while primarily addressing the morbid anatomist and histopathologist, also provides a valuable source of reference for obstetricians, neonatologists and paediatricians. Its value as a working tool is enhanced by effective cross-referencing, by chapter and page number, and a detailed index.

Keywords

Medicine & Public Health. --- Pathology. --- Obstetrics/Perinatology. --- Pediatrics. --- Anatomy. --- Medicine. --- Human anatomy. --- Obstetrics. --- Médecine --- Anatomie humaine --- Obstétrique --- Pathologie --- Pédiatrie --- Autopsy -- Methods. --- Congenital Abnormalities -- Pathology. --- Fetal Diseases -- Pathology. --- Fetus -- Abnormalities. --- Fetus -- Diseases. --- Fetus -- Pathophysiology. --- Infant, Newborn, Diseases -- Pathology. --- Newborn infants -- Diseases. --- Pediatric pathology. --- Fetus --- Newborn infants --- Pediatric pathology --- Fetal Diseases --- Congenital Abnormalities --- Autopsy --- Infant, Newborn, Diseases --- Pathology --- Methods --- Investigative Techniques --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Medicine --- Forensic Medicine --- Pregnancy Complications --- Female Urogenital Diseases and Pregnancy Complications --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Diseases --- Health Occupations --- Forensic Sciences --- Criminology --- Disciplines and Occupations --- Social Sciences --- Anthropology, Education, Sociology and Social Phenomena --- Gynecology & Obstetrics --- Health & Biological Sciences --- Abnormalities --- Pathophysiology --- Diseases. --- Abnormalities. --- Pathophysiology. --- Fetal pathophysiology --- Fetal physiopathology --- Embryopathies --- Physiopathology --- Abnormities and deformities --- Physiology, Pathological --- Abnormalities, Human --- Pregnancy --- Complications --- Obstetrics/Perinatology/Midwifery. --- Anatomy, Human --- Anatomy --- Human biology --- Medical sciences --- Human body --- Disease (Pathology) --- Medicine, Preventive --- Paediatrics --- Pediatric medicine --- Children --- Maternal-fetal medicine --- Health and hygiene

Neurogenetic developmental disorders : variation of manifestation in childhood
Authors: ---
ISBN: 0262134802 9786612098857 0262279320 1282098853 1429477156 0262293242 9780262279321 9781429477154 9781282098855 9780262134804 Year: 2007 Publisher: Cambridge, Massachusetts ; London : The MIT Press,

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Abstract

A reference to guide clinicians, researchers, teachers, and parents in identifying a range of genetic disorders despite widely variable cognitive, behavioral, and physical effects.

Keywords

Chromosome abnormalities. --- Developmental disabilities -- Genetic aspects. --- Neurogenetics. --- Pediatric neuropsychology. --- Developmental disabilities --- Chromosome abnormalities --- Neurogenetics --- Pediatric neuropsychology --- Sex Chromosome Disorders --- Methods --- Heredodegenerative Disorders, Nervous System --- Diagnosis --- Genetic Diseases, Inborn --- Genetic Counseling --- Child --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Investigative Techniques --- Age Groups --- Chromosome Disorders --- Genetics, Medical --- Neurodegenerative Diseases --- Genetic Services --- Persons --- Nervous System Diseases --- Congenital Abnormalities --- Health Services --- Diseases --- Genetics --- Health Care Facilities, Manpower, and Services --- Named Groups --- Biology --- Biological Science Disciplines --- Health Care --- Natural Science Disciplines --- Disciplines and Occupations --- Pediatrics --- Medicine --- Health & Biological Sciences --- Genetic aspects --- Genetic aspects. --- Child neuropsychology --- Developmental neuropsychology --- Nervous system --- Chromosomal aberrations --- Chromosome anomalies --- Neuropsychology --- Pediatric neurology --- Neurosciences --- Chromosomes --- Karyotypes --- Mutation (Biology) --- Disabilities --- Developmentally disabled --- NEUROSCIENCE/General --- Introducción a la Psicobiología del Desarrollo (14102205) |x Bibliografía recomendada --- Enfant --- Développement --- Syndrome d'origine génétique --- Neuropsychopathologie --- développement --- trouble --- Developmental disabilities. --- Troubles du développement. --- Génétique

Androgen Excess Disorders in Women
Author:
ISBN: 1588296636 9786610832552 128083255X 1597451797 Year: 2007 Publisher: Totowa, NJ : Humana Press : Imprint: Humana,

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Abstract

The field of androgen excess disorders has advanced substantially since the original publication of this book. The Androgen Excess Society (AES) was founded to bring together investigators in the field. A better understanding of the screening, progression, and molecular genetics of nonclassic adrenal hyperplasia (NCAH) has improved the clinical care and diagnostic accuracy of these patients. New criteria for the diagnosis of the polycystic ovary syndrome (PCOS) were proposed in Rotterdam, criteria that have resulted in controversy and, hopefully, initiation of new studies. The association of insulin resistance with PCOS has been strengthened, and the role of metformin in tre- ing the infertility of the PCOS has been validated. Risks for diabetes and, more cont- versially, cardiovascular disease in women with PCOS have received substantial investigation. Our understanding of the epidemiology and economic impact of these disorders has expanded, emphasizing their critical importance. These are but a few highlights of how the terrain has changed in a relatively brief period of time. In keeping with these advances, the title of this book has been revised to reflect the growing importance of PCOS as the most prevalent androgen excess disorder in women, and arguably, as the one that might have the most serious adverse consequences for general health. There are fewer chapters to provide a more focused elucidation of the area. Several chapters were penned by new (and young) authors who are conducting cutting-edge research in the field.

Keywords

Adrenal glands. --- Adrenal glands --- Androgens --- Polycystic ovary syndrome --- Adrenogenital Syndrome --- Adrenal Gland Diseases --- Ovarian Cysts --- Hormones --- 46, XX Disorders of Sex Development --- Disorders of Sex Development --- Ovarian Diseases --- Hormones, Hormone Substitutes, and Hormone Antagonists --- Cysts --- Endocrine System Diseases --- Adnexal Diseases --- Urogenital Abnormalities --- Gonadal Disorders --- Physiological Effects of Drugs --- Neoplasms --- Diseases --- Congenital Abnormalities --- Female Urogenital Diseases --- Pharmacologic Actions --- Male Urogenital Diseases --- Genital Diseases, Female --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Chemical Actions and Uses --- Female Urogenital Diseases and Pregnancy Complications --- Chemicals and Drugs --- Hyperandrogenism --- Polycystic Ovary Syndrome --- Adrenocortical Hyperfunction --- Medicine --- Health & Biological Sciences --- Clinical Endocrinology --- Gynecology & Obstetrics --- Metabolism --- Physiological effect --- Disorders, Congenital --- Congenital Disorders --- Neonatal Diseases and Abnormalities --- Congenital Disorder --- Disorder, Congenital --- Female Genital Diseases --- Gynecologic Diseases --- Diseases, Female Genital --- Diseases, Gynecologic --- Female Genital Disease --- Genital Disease, Female --- Gynecologic Disease --- Male Genitourinary Diseases --- Genitourinary Disease, Male --- Genitourinary Diseases, Male --- Male Genitourinary Disease --- Male Urogenital Disease --- Urogenital Disease, Male --- Urogenital Diseases, Male --- Chemical Actions --- Actions, Chemical --- Actions, Pharmacologic --- Female Genitourinary Diseases --- Female Genitourinary Disease --- Female Urogenital Disease --- Genitourinary Disease, Female --- Genitourinary Diseases, Female --- Urogenital Disease, Female --- Urogenital Diseases, Female --- Abnormalities, Congenital --- Defects, Congenital --- Birth Defects --- Congenital Defects --- Deformities --- Abnormality, Congenital --- Birth Defect --- Congenital Abnormality --- Congenital Defect --- Defect, Birth --- Defect, Congenital --- Defects, Birth --- Deformity --- Benign Neoplasms --- Malignancy --- Neoplasia --- Neoplasm --- Neoplasms, Benign --- Cancer --- Tumors --- Benign Neoplasm --- Cancers --- Malignancies --- Neoplasias --- Neoplasm, Benign --- Tumor --- Drug Effects on Physiology --- Drug Physiological Effects --- Effects, Drug Physiological --- Physiological Effects, Drug --- Disorder, Gonadal --- Disorders, Gonadal --- Gonadal Disorder --- Abnormalities, Urogenital --- Genitourinary Abnormalities --- Abnormalities, Genitourinary --- Abnormality, Genitourinary --- Abnormality, Urogenital --- Genitourinary Abnormality --- Urogenital Abnormality --- Urogenital System --- Adnexal Disease --- Disease, Adnexal --- Diseases, Adnexal --- Diseases of Endocrine System --- Endocrine Diseases --- Disease, Endocrine --- Disease, Endocrine System --- Diseases, Endocrine --- Diseases, Endocrine System --- Endocrine Disease --- Endocrine System Disease --- System Disease, Endocrine --- System Diseases, Endocrine --- Cyst --- Hormones, Substitutes, Antagonists --- Disease, Ovarian --- Diseases, Ovarian --- Ovarian Disease --- Ambiguous Genitalia --- Genital Ambiguity --- Hermaphroditism --- Intersex Conditions --- Intersexuality --- Pseudohermaphroditism --- Sexual Development Disorders --- Sexual Differentiation Disorders --- Disorders of Sexual Development --- Sex Development Disorders --- Sex Differentiation Disorders --- Ambiguities, Genital --- Ambiguity, Genital --- Condition, Intersex --- Conditions, Intersex --- Differentiation Disorder, Sex --- Differentiation Disorder, Sexual --- Differentiation Disorders, Sex --- Differentiation Disorders, Sexual --- Disorder, Sex Differentiation --- Disorder, Sexual Differentiation --- Disorders, Sex Differentiation --- Disorders, Sexual Differentiation --- Genital Ambiguities --- Genitalia, Ambiguous --- Intersex Condition --- Intersexualities --- Sex Development Disorder --- Sex Differentiation Disorder --- Sexual Development Disorder --- Sexual Differentiation Disorder --- Hormone --- Hormone Receptor Agonists --- Agonists, Hormone Receptor --- Receptor Agonists, Hormone --- Corpus Luteum Cyst --- Corpus Luteum Cysts --- Cyst, Corpus Luteum --- Cyst, Ovarian --- Cysts, Corpus Luteum --- Cysts, Ovarian --- Ovarian Cyst --- Adrenal Gland Disease --- Disease, Adrenal Gland --- Diseases, Adrenal Gland --- Gland Disease, Adrenal --- Gland Diseases, Adrenal --- PCOD (Gynecology) --- PCOS (Gynecology) --- Polycystic ovarian disease --- Polyfollicular ovarian disease --- Sclerocystic ovarian degeneration --- Sclerocystic ovaries --- Sclerocystic ovary syndrome --- Stein-Leventhal syndrome --- Androgenic hormones --- Adrenal Gland Hyperfunction --- Hyperadrenalism --- Hyperadrenocorticism --- Hypercorticism --- Hyperfunction, Adrenal Gland --- Hyperfunction, Adrenocortical --- Androgen Effect --- Androgen Effects --- Androgen Receptor Agonists --- Androgenic Agents --- Androgenic Compounds --- Agents, Androgenic --- Agonists, Androgen Receptor --- Compounds, Androgenic --- Effect, Androgen --- Effects, Androgen --- Receptor Agonists, Androgen --- Receptors, Androgen --- Polycystic Ovarian Syndrome --- Polycystic Ovary Syndrome 1 --- Sclerocystic Ovarian Degeneration --- Sclerocystic Ovaries --- Sclerocystic Ovary Syndrome --- Stein-Leventhal Syndrome --- Ovarian Degeneration, Sclerocystic --- Ovarian Syndrome, Polycystic --- Ovary Syndrome, Polycystic --- Ovary, Sclerocystic --- Sclerocystic Ovary --- Stein Leventhal Syndrome --- Syndrome, Polycystic Ovary --- Syndrome, Stein-Leventhal --- abnormalities --- agonists --- 46, XX DSD --- 46,XX DSD --- 46,XX Disorders of Sex Development --- Female Pseudohermaphroditism --- Female Pseudohermaphroditisms --- Pseudohermaphroditism, Female --- Pseudohermaphroditisms, Female --- Adrenogenital Syndromes --- Syndrome, Adrenogenital --- Syndromes, Adrenogenital --- Medicine. --- Endocrinology. --- Medicine & Public Health. --- Internal medicine --- Endocrinology .

Spinocerebellar degenerations : the ataxias and spastic paraplegias
Authors: --- ---
ISBN: 0750675039 9780750675031 9780702038938 0702038938 Year: 2007 Publisher: [Place of publication not identified] Butterworth Heinemann/Elsevier

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Abstract

Keywords

Cerebellar ataxia --- Paralysis, Spastic --- Hereditary Sensory and Motor Neuropathy --- Ataxia --- Heredodegenerative Disorders, Nervous System --- Cerebellar Diseases --- Spinal Cord Diseases --- Neurodegenerative Diseases --- Polyneuropathies --- Central Nervous System Diseases --- Brain Diseases --- Genetic Diseases, Inborn --- Nervous System Malformations --- Dyskinesias --- Peripheral Nervous System Diseases --- Neurologic Manifestations --- Nervous System Diseases --- Congenital Abnormalities --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Diseases --- Signs and Symptoms --- Neuromuscular Diseases --- Pathological Conditions, Signs and Symptoms --- Cerebellar Ataxia --- Spastic Paraplegia, Hereditary --- Spinocerebellar Degenerations --- Medicine --- Health & Biological Sciences --- Neurology --- Early Onset Cerebellar Ataxia --- Familial Spinocerebellar Degenerations --- Garland-Moorhouse Syndrome --- Hereditary Oligophrenic Cerebello-Lental Degeneration --- Hereditary Spinocerebellar Degenerations --- Inherited Spinocerebellar Degenerations --- Late Onset Cerebellar Ataxia --- Marie's Cerebellar Ataxia --- Marinesco-Garland Syndrome --- Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism --- Marinesco-Sjogren Syndrome-Myopathy --- Marinesco-Sjogren-Garland Syndrome --- Marinesco-Sjögren Syndrome --- Spino Cerebellar Degenerations --- Spino-Cerebellar Degenerations --- Spinocerebellar Diseases --- Ataxias, Hereditary --- Cerebellar Ataxia, Early Onset --- Cerebellar Ataxia, Late Onset --- Cerebellar Degenerations, Primary --- Corticostriatal-Spinal Degeneration --- Marie Cerebellar Ataxia --- Marinesco-Sjogren Syndrome --- Spinocerebellar Degeneration --- Ataxia, Hereditary --- Cerebellar Ataxia, Marie --- Cerebellar Ataxia, Marie's --- Cerebellar Degeneration, Primary --- Corticostriatal Spinal Degeneration --- Corticostriatal-Spinal Degenerations --- Degeneration, Corticostriatal-Spinal --- Degeneration, Familial Spinocerebellar --- Degeneration, Hereditary Spinocerebellar --- Degeneration, Inherited Spinocerebellar --- Degeneration, Primary Cerebellar --- Degeneration, Spino Cerebellar --- Degeneration, Spino-Cerebellar --- Degeneration, Spinocerebellar --- Degenerations, Corticostriatal-Spinal --- Degenerations, Familial Spinocerebellar --- Degenerations, Hereditary Spinocerebellar --- Degenerations, Inherited Spinocerebellar --- Degenerations, Primary Cerebellar --- Degenerations, Spino Cerebellar --- Degenerations, Spinocerebellar --- Familial Spinocerebellar Degeneration --- Garland Moorhouse Syndrome --- Hereditary Ataxia --- Hereditary Ataxias --- Hereditary Oligophrenic Cerebello Lental Degeneration --- Hereditary Spinocerebellar Degeneration --- Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic --- Inherited Spinocerebellar Degeneration --- Marinesco Garland Syndrome --- Marinesco Sjogren Garland Syndrome --- Marinesco Sjogren Syndrome --- Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism --- Marinesco Sjogren Syndrome Myopathy --- Marinesco Sjögren Syndrome --- Primary Cerebellar Degeneration --- Primary Cerebellar Degenerations --- Spino Cerebellar Degeneration --- Spino-Cerebellar Degeneration --- Spinocerebellar Degeneration, Familial --- Spinocerebellar Degeneration, Hereditary --- Spinocerebellar Degeneration, Inherited --- Spinocerebellar Degenerations, Familial --- Spinocerebellar Degenerations, Hereditary --- Spinocerebellar Degenerations, Inherited --- Spinocerebellar Disease --- Syndrome, Garland-Moorhouse --- Syndrome, Marinesco-Garland --- Syndrome, Marinesco-Sjogren --- Syndrome, Marinesco-Sjogren-Garland --- Syndrome, Marinesco-Sjögren --- Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren --- Syndrome-Myopathy, Marinesco-Sjogren --- Autosomal Dominant Hereditary Spastic Paraplegia --- Autosomal Dominant Spastic Paraplegia Hereditary --- Autosomal Recessive Hereditary Spastic Paraplegia --- Autosomal Recessive Spastic Paraplegia, Hereditary --- CMT with Pyramidal Features --- Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant --- HMSN 5 --- HMSN Type V --- HMSN V --- HMSN V (Hereditary Motor and Sensory Neuropathy Type V) --- Hereditary Autosomal Dominant Spastic Paraplegia --- Hereditary Autosomal Recessive Spastic Paraplegia --- Hereditary Motor And Sensory Neuropathy V --- Hereditary Motor and Sensory Neuropathy 5 --- Hereditary Motor-Sensory Neuropathy with Pyramidal Signs --- Hereditary Spastic Paraplegia, Autosomal Recessive --- Hereditary X-Linked Recessive Spastic Paraplegia --- Hereditary, Spastic Paraplegia, Autosomal Dominant --- Hereditary, Spastic Paraplegia, X-Linked Recessive --- Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia --- Paraplegia, Spastic, Hereditary --- Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant --- Spastic Paraplegia 2 --- Spastic Paraplegia Type 2 --- Spastic Paraplegia, Autosomal Dominant, Hereditary --- Spastic Paraplegia, Autosomal Recessive, Hereditary --- Spastic Paraplegia, Hereditary, Autosomal Dominant --- Spastic Paraplegia, Hereditary, Autosomal Recessive --- Spastic Paraplegia, Hereditary, X-Linked Recessive --- Spastic Paraplegia, X-Linked Recessive, Hereditary --- Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy --- Type V Hereditary Motor and Sensory Neuropathy --- X Linked Recessive Hereditary Spastic Paraplegia --- X-linked Recessive Hereditary Spastic Paraplegia --- Hereditary Spastic Paraplegia --- X-Linked, Spastic Paraplegia, Hereditary --- Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant --- Hereditary Motor Sensory Neuropathy with Pyramidal Signs --- Hereditary Spastic Paraplegias --- Hereditary X Linked Recessive Spastic Paraplegia --- Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia --- Paraplegia, Hereditary Spastic --- Paraplegias, Hereditary Spastic --- Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy --- Spastic Paraplegias, Hereditary --- Type V, HMSN --- Cerebellar Hemiataxia --- Cerebellar Incoordination --- Hypermetria --- Adiadochokinesis --- Ataxia, Cerebellar --- Cerebellar Dysmetria --- Dysmetria --- Adiadochokineses --- Ataxias, Cerebellar --- Cerebellar Ataxias --- Cerebellar Dysmetrias --- Cerebellar Hemiataxias --- Cerebellar Incoordinations --- Dysmetria, Cerebellar --- Dysmetrias --- Dysmetrias, Cerebellar --- Hemiataxia, Cerebellar --- Hemiataxias, Cerebellar --- Hypermetrias --- Incoordination, Cerebellar --- Incoordinations, Cerebellar --- Symptoms and General Pathology --- Cramp-Fasciculation Syndrome --- Fasciculation-Cramp Syndrome, Benign --- Foley-Denny-Brown Syndrome --- Oppenheim's Disease --- Amyotonia Congenita --- Oppenheim Disease --- Benign Fasciculation-Cramp Syndrome --- Benign Fasciculation-Cramp Syndromes --- Cramp Fasciculation Syndrome --- Cramp-Fasciculation Syndromes --- Fasciculation Cramp Syndrome, Benign --- Fasciculation-Cramp Syndromes, Benign --- Foley Denny Brown Syndrome --- Neuromuscular Disease --- Oppenheims Disease --- Syndrome, Cramp-Fasciculation --- Syndrome, Foley-Denny-Brown --- Syndromes, Cramp-Fasciculation --- Symptoms and Signs --- Disorders, Congenital --- Congenital Disorders --- Neonatal Diseases and Abnormalities --- Congenital Disorder --- Disorder, Congenital --- Abnormalities, Congenital --- Defects, Congenital --- Birth Defects --- Congenital Defects --- Deformities --- Abnormality, Congenital --- Birth Defect --- Congenital Abnormality --- Congenital Defect --- Defect, Birth --- Defect, Congenital --- Defects, Birth --- Deformity --- Fetal Diseases --- Infant, Newborn, Diseases --- Teratogenesis --- Nervous System Disorders --- Neurological Disorders --- Neurologic Disorders --- Disease, Nervous System --- Diseases, Nervous System --- Disorder, Nervous System --- Disorder, Neurologic --- Disorder, Neurological --- Disorders, Nervous System --- Disorders, Neurologic --- Disorders, Neurological --- Nervous System Disease --- Nervous System Disorder --- Neurologic Disorder --- Neurological Disorder --- Focal Neurologic Deficits --- Manifestations, Neurologic --- Manifestations, Neurological --- Neurologic Dysfunction --- Neurologic Findings --- Neurologic Manifestation --- Neurologic Signs --- Neurologic Symptoms --- Neurological Manifestations --- Neurologic Deficits --- Neurologic Signs and Symptoms --- Deficit, Focal Neurologic --- Deficit, Neurologic --- Deficits, Focal Neurologic --- Deficits, Neurologic --- Dysfunction, Neurologic --- Dysfunctions, Neurologic --- Finding, Neurologic --- Findings, Neurologic --- Focal Neurologic Deficit --- Manifestation, Neurologic --- Manifestation, Neurological --- Neurologic Deficit --- Neurologic Deficit, Focal --- Neurologic Deficits, Focal --- Neurologic Dysfunctions --- Neurologic Finding --- Neurologic Sign --- Neurologic Symptom --- Neurological Manifestation --- Sign, Neurologic --- Signs, Neurologic --- Symptom, Neurologic --- Symptoms, Neurologic --- Nervous System --- PNS (Peripheral Nervous System) Diseases --- PNS Diseases --- Peripheral Nervous System Disease --- Peripheral Nervous System Disorders --- Peripheral Nerve Diseases --- Peripheral Neuropathies --- Nerve Disease, Peripheral --- Nerve Diseases, Peripheral --- Neuropathy, Peripheral --- PNS Disease --- Peripheral Nerve Disease --- Peripheral Neuropathy --- Abnormal Movements --- Hemiballism --- Linguofacial Dyskinesia --- Oral Dyskinesia --- Oral-Facial Dyskinesia --- Tardive Oral Dyskinesia --- Asterixis --- Ballismus --- Hemiballismus --- Involuntary Movements --- Lingual-Facial-Buccal Dyskinesia --- Orofacial Dyskinesia --- Abnormal Movement --- Dyskinesia --- Dyskinesia, Lingual-Facial-Buccal --- Dyskinesia, Linguofacial --- Dyskinesia, Oral --- Dyskinesia, Oral-Facial --- Dyskinesia, Orofacial --- Dyskinesias, Lingual-Facial-Buccal --- Dyskinesias, Linguofacial --- Dyskinesias, Oral --- Dyskinesias, Oral-Facial --- Dyskinesias, Orofacial --- Involuntary Movement --- Lingual Facial Buccal Dyskinesia --- Lingual-Facial-Buccal Dyskinesias --- Linguofacial Dyskinesias --- Movement, Abnormal --- Movement, Involuntary --- Movements, Abnormal --- Movements, Involuntary --- Oral Dyskinesias --- Oral Facial Dyskinesia --- Oral-Facial Dyskinesias --- Orofacial Dyskinesias --- Tardive Oral Dyskinesias --- Movement Disorders --- Abnormalities, Congenital, Nervous System --- Abnormalities, Nervous System --- Anomalies, Nervous System --- Congenital Abnormalities, Nervous System --- Congenital Anomalies, Nervous System --- Congenital Malformations, Nervous System --- Cranioschisis --- Malformations, Nervous System, Congenital --- Nervous System Anomalies --- Nervous System Congenital Abnormalities --- Nervous System Congenital Malformations --- Nervous System Malformations, Congenital --- Nervous System Abnormalities --- Abnormality, Nervous System --- Anomaly, Nervous System --- Cranioschises --- Malformation, Nervous System --- Malformations, Nervous System --- Nervous System Abnormality --- Nervous System Anomaly --- Nervous System Malformation --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Genetics, Medical --- Brain Disorders --- CNS Disorders, Intracranial --- Central Nervous System Disorders, Intracranial --- Central Nervous System Intracranial Disorders --- Encephalon Diseases --- Encephalopathy --- Intracranial CNS Disorders --- Intracranial Central Nervous System Disorders --- Brain Disease --- Brain Disorder --- CNS Disorder, Intracranial --- Encephalon Disease --- Encephalopathies --- Intracranial CNS Disorder --- CNS Diseases --- Central Nervous System Disorders --- CNS Disease --- Polyneuropathy, Critical Illness --- Polyneuropathy, Familial --- Polyneuropathy, Inherited --- Polyneuropathy, Motor --- Polyneuropathy, Acquired --- Acquired Polyneuropathies --- Acquired Polyneuropathy --- Critical Illness Polyneuropathies --- Critical Illness Polyneuropathy --- Familial Polyneuropathies --- Familial Polyneuropathy --- Inherited Polyneuropathies --- Inherited Polyneuropathy --- Motor Polyneuropathies --- Motor Polyneuropathy --- Polyneuropathies, Acquired --- Polyneuropathies, Critical Illness --- Polyneuropathies, Familial --- Polyneuropathies, Inherited --- Polyneuropathies, Motor --- Polyneuropathy --- Degenerative Diseases, Central Nervous System --- Degenerative Diseases, Neurologic --- Degenerative Diseases, Spinal Cord --- Degenerative Neurologic Diseases --- Degenerative Neurologic Disorders --- Nervous System Degenerative Diseases --- Neurodegenerative Disorders --- Neurologic Degenerative Conditions --- Neurologic Degenerative Diseases --- Neurologic Diseases, Degenerative --- Degenerative Diseases, Nervous System --- Degenerative Condition, Neurologic --- Degenerative Conditions, Neurologic --- Degenerative Neurologic Disease --- Degenerative Neurologic Disorder --- Neurodegenerative Disease --- Neurodegenerative Disorder --- Neurologic Degenerative Condition --- Neurologic Degenerative Disease --- Neurologic Disease, Degenerative --- Neurologic Disorder, Degenerative --- Neurologic Disorders, Degenerative --- Spinal Cord Disorders --- Myelopathy --- Myelopathies --- Spinal Cord Disease --- Spinal Cord Disorder --- Cerebellar Disorders --- Cerebellar Syndromes --- Cerebellar Dysfunction --- Cerebellum Diseases --- Cerebellar Disease --- Cerebellar Disorder --- Cerebellar Dysfunctions --- Cerebellar Syndrome --- Cerebellum Disease --- Disease, Cerebellar --- Disease, Cerebellum --- Disorder, Cerebellar --- Dysfunction, Cerebellar --- Syndrome, Cerebellar --- Degenerative Hereditary Diseases, Nervous System --- Hereditary Neurodegenerative Diseases --- Hereditary-Degenerative Disorders, Nervous System --- Nervous System Degenerative Hereditary Diseases --- Nervous System Hereditary Degenerative Diseases --- Degenerative Disease, Nervous System, Hereditary --- Degenerative Hereditary Disorders, Nervous System --- Hereditary Diseases, Neurodegenerative --- Nervous System Diseases, Degenerative, Hereditary --- Neurodegenerative Diseases, Hereditary --- Disease, Hereditary Neurodegenerative --- Disease, Neurodegenerative Hereditary --- Diseases, Hereditary Neurodegenerative --- Diseases, Neurodegenerative Hereditary --- Hereditary Degenerative Disorders, Nervous System --- Hereditary Disease, Neurodegenerative --- Hereditary Neurodegenerative Disease --- Neurodegenerative Disease, Hereditary --- Neurodegenerative Hereditary Disease --- Neurodegenerative Hereditary Diseases --- Ataxia, Appendicular --- Ataxia, Limb --- Ataxia, Motor --- Ataxia, Sensory --- Ataxia, Truncal --- Ataxy --- Dyscoordination --- Lack of Coordination --- Tremor, Rubral --- Coordination Impairment --- Dyssynergia --- Incoordination --- Appendicular Ataxia --- Appendicular Ataxias --- Ataxias --- Ataxias, Appendicular --- Ataxias, Limb --- Ataxias, Motor --- Ataxias, Sensory --- Ataxias, Truncal --- Coordination Impairments --- Coordination Lack --- Impairment, Coordination --- Impairments, Coordination --- Incoordinations --- Limb Ataxia --- Limb Ataxias --- Motor Ataxia --- Motor Ataxias --- Rubral Tremor --- Rubral Tremors --- Sensory Ataxia --- Sensory Ataxias --- Tremors, Rubral --- Truncal Ataxia --- Truncal Ataxias --- CMT4f --- Charcot-Marie-Tooth Disease, Demyelinating, Type 4f --- Charcot-Marie-Tooth Disease, Type 3 --- Dejerine-Sottas Neuropathy --- Dejerine-Sottas Syndrome --- HMSN3 --- Herditary Sensory and Motor Neuropathy --- Hereditary Motor and Sensory Neuropathy --- Hereditary Motor and Sensory Neuropathy 3 --- Hereditary Motor and Sensory Neuropathy Type III --- Hypertrophic Neuropathy of Dejerine-Sottas --- Dejerine-Sottas Disease --- HMSN --- HMSN Type III --- HMSN Type VII --- Hereditary Motor and Sensory Neuropathies --- Hereditary, Type III, Motor and Sensory Neuropathy --- Hereditary, Type VII, Motor and Sensory Neuropathy --- Neuropathies, Hereditary Motor and Sensory --- Charcot Marie Tooth Disease, Type 3 --- Dejerine Sottas Disease --- Dejerine Sottas Neuropathy --- Dejerine Sottas Syndrome --- Dejerine-Sottas Hypertrophic Neuropathy --- Disease, Dejerine-Sottas --- HMSN Type IIIs --- HMSN Type VIIs --- Hypertrophic Neuropathy of Dejerine Sottas --- Neuropathy, Dejerine-Sottas --- Syndrome, Dejerine-Sottas --- Type VII, HMSN --- Spastic paralysis --- Neuromuscular diseases --- Spasticity --- Cerebellum --- abnormalities --- Fetal Anomalies --- Fetal Malformations --- Anomaly, Fetal --- Fetal Anomaly --- Fetal Malformation --- Malformation, Fetal --- Central Nervous System Disease --- Central Nervous System Disorder

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