Pages with the most revisions
Showing below up to 50 results starting with #1.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)
- Creatine Deficiency Syndromes (156 revisions)
- Disseminated encephalomyelitis in children (81 revisions)
- Anti NMDAR encephalitis (77 revisions)
- Cerebrovascular disease and stroke (67 revisions)
- DNA Polymerase gamma and mitochondrial replication disorders (62 revisions)
- Main Page (49 revisions)
- Cerebral venous sinus thrombosis (44 revisions)
- Paediatric migraine (44 revisions)
- Comparitive genomic hybridization (43 revisions)
- Congenital Disorders of Glycosylation (39 revisions)
- Birt-Hogg-Dube syndrome (38 revisions)
- Dilated Cardiomyopathy (37 revisions)
- Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive (37 revisions)
- Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant (36 revisions)
- Inherited disorders of the Urea Cycle (30 revisions)
- Mitochondrial Disorders (27 revisions)
- Long term safety of ketogenic diet (27 revisions)
- Paroxysmal nonepileptic disorders (26 revisions)
- Disorders of metabolism and neurodegenerative disorders associated with epilepsy (24 revisions)
- Retinitis Pigmentosa, Autosomal Dominant (24 revisions)
- Charcot-Marie-Tooth Neuropathy Type 2 (24 revisions)
- Retinitis Pigmentosa, Autosomal Recessive (23 revisions)
- Febrile seizures (23 revisions)
- Bacterial meningitis (22 revisions)
- Familial Hypertrophic Cardiomyopathy (21 revisions)
- Leber Congenital Amaurosis (21 revisions)
- ILAE Classification and Terminology of Seizures and Epilepsies (21 revisions)
- Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy, Autosomal Dominant (20 revisions)
- Primary Ciliary Dyskinesia (20 revisions)
- Fever induced refractory epileptic encephalopathy in school age children (20 revisions)
- Mit (19 revisions)
- Neuronal Ceroid-Lipofuscinoses (19 revisions)
- Joubert Syndrome (19 revisions)
- Charcot-Marie-Tooth Neuropathy Type 4 (18 revisions)
- Fanconi Anemia (18 revisions)
- Urea Cycle Disorders (16 revisions)
- Parkinson Disease (16 revisions)
- Holoprosencephaly (16 revisions)
- Bardet-Biedl Syndrome (15 revisions)
- Cleft Lip +/- Cleft Palate (15 revisions)
- Zellweger Syndrome Spectrum (15 revisions)
- Long-term efficacy of valproate versus lamotrigine in treatment of idiopathic generalized epilepsies in children and adolescents (15 revisions)
- Age-Related Macular Degeneration (15 revisions)
- Leigh Syndrome (nuclear DNA mutation) (15 revisions)
- Amyotrophic Lateral Sclerosis (15 revisions)
- Diamond-Blackfan Anemia (15 revisions)
- Eosinophilic meningitis (14 revisions)
- Limb-Girdle Muscular Dystrophy (14 revisions)
- Xeroderma Pigmentosum (14 revisions)
- Mitochondrial DNA-Associated Leigh Syndrome and NARP (14 revisions)
