发文地区与机构
近年国家 / 地区发文量统计
| 国家 / 地区 | 发文量 |
|---|---|
| GERMANY (FED REP GER) | 82 |
| USA | 36 |
| Italy | 33 |
| Austria | 24 |
| Netherlands | 24 |
| France | 23 |
| Switzerland | 22 |
| India | 19 |
| England | 15 |
| Turkey | 14 |
近年机构发文量统计
| 机构 | 发文量 |
|---|---|
| EBERHARD KARLS UNIVERSITY OF TUBINGEN | 14 |
| PARACELSUS PRIVATE MEDICAL UNIVERSITY | 14 |
| UNIVERSITY OF MUNICH | 13 |
| TECHNICAL UNIVERSITY OF MUNICH | 11 |
| UNIVERSITY CHILDREN'S HOSPITAL ZURICH | 11 |
| INSTITUT NATIONAL DE LA SANTE ET DE LA ... | 9 |
| POST GRADUATE INSTITUTE OF MEDICAL EDUC... | 8 |
| VRIJE UNIVERSITEIT AMSTERDAM | 8 |
| CHU DE TOULOUSE | 6 |
| HELMHOLTZ ASSOCIATION | 6 |
文章引用情况
1
Febrile Infection-Related Epilepsy Syndrome (FIRES) with Multifocal Subcortical Infarcts, A New Imaging Phenotype2
X-linked Charcot-Marie-Tooth Disease Presenting with Stuttering Stroke-like Symptoms3
Low Voice, Spasmodic Dysphonia, and Hand Dystonia as Clinical Clues for KMT2B-Associated Early-Onset Dystonia4
Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience5
A Very Rare Etiology of Hypotonia and Seizures: Congenital Glutamine Synthetase Deficiency6
Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review7
B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss8
Assessing and Improving Documentation of Pediatric Brain Death Determination within an Electronic Health Record9
Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature10
Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients