All Stories

  1. In Memoriam: Alan Aron, MD (October 15, 1933–December 26, 2017)*
  2. In Memoriam
  3. Acute Encephalopathy With Biphasic Seizures and Late Restricted Diffusion
  4. Expanding Phenotypic Spectrum of NKX2-1 –Related Disorders—Mitochondrial and Immunologic Dysfunction
  5. Whole Exome Sequencing and Heterologous Cellular Electrophysiology Studies Elucidate a Novel Loss-of-Function Mutation in the CACNA1A-Encoded Neuronal P/Q-Type Calcium Channel in a Child With Congenital Hypotonia and Developmental Delay
  6. Too Old for a Diaper! A Child With Diaper Changing–Induced Seizures
  7. Peer review fraud—it’s not big and it’s not clever
  8. Quo vadis: the re-definition of “inborn metabolic diseases”
  9. Impaired glycosylation has widepsread effects on the nervous system
  10. Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study
  11. Case definition and classification of leukodystrophies and leukoencephalopathies
  12. JIMD Reports, Volume 21
  13. JIMD Reports, Volume 20
  14. JIMD Reports, Volume 18
  15. JIMD Reports, Volume 22
  16. JIMD Reports, Volume 19
  17. JIMD Reports, Volume 23
  18. JIMD Reports, Volume 24
  19. Peripheral Neuropathy in Inherited Metabolic Disease
  20. Congenital Disorders of N-linked Glycosylation
  21. Substrate Deprivation Therapy
  22. Editorial Comment: Ataxia, Ophthalmoplegia, and Impairment of Consciousness in a 19 Month-Old American Boy
  23. Editorial Comment: Cerebellar Ataxia, Vertical Supranuclear Gaze Palsy, Sensorineural Deafness, Epilepsy, Dementia and Hallucinations in an Adolescent Male
  24. A 19-Month-Old Girl of South Indian Parents Presented to a General Pediatric Clinic for Evaluation of Global Developmental Regression
  25. Longitudinal study of cognition in Niemann-Pick disease type C
  26. Longitudinal data from the international registry for Niemann-Pick disease type C (NPC)
  27. Niemann-Pick type C Suspicion Index tool: analyses by age and association of manifestations
  28. Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation
  29. Proton Magnetic Resonance Spectroscopy as a Probe into the Pathophysiology of Autism Spectrum Disorders (ASD): A Review
  30. Posterior reversible encephalopathy syndrome and hemorrhage associated with tacrolimus in a pediatric heart transplantation recipient
  31. Gangliosidoses
  32. Correction: Disease and patient characteristics in NP-C patients: findings from an international disease registry
  33. Disease and patient characteristics in NP-C patients: findings from an international disease registry
  34. Niemann-Pick Disease Type C
  35. Neurotransmitter abnormalities and response to supplementation in SPG11
  36. Recommendations for the diagnosis and management of Niemann–Pick disease type C: An update
  37. Neurology of inherited glycosylation disorders
  38. Longitudinal Study of Cognition in Patients with Niemann-Pick Disease, Type C
  39. Update From the International Registry for Niemann-Pick Disease Type C (NP-C) in Clinical Practice
  40. Disorders of Glycosylation
  41. Diseases Associated with Primary Abnormalities in Carbohydrate Metabolism
  42. Dysphagia as a risk factor for mortality in Niemann-Pick disease type C: systematic literature review and evidence from studies with miglustat
  43. Inborn Errors of Metabolism for Child Neurology Residents
  44. Co-morbidity of Sanfilippo Syndrome type C and d-2-hydroxyglutaric aciduria
  45. Longitudinal study of cognition in Niemann-Pick Disease, Type C
  46. ZOOM: Observational genetic screening study of Niemann-Pick Disease Type C in adults with neurological and psychiatric signs
  47. Baseline data from a prospective international disease registry for Niemann-Pick disease type C
  48. Miglustat in adult and juvenile patients with Niemann–Pick disease type C: Long-term data from a clinical trial
  49. Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNALeu(CUN) gene
  50. 106. Longitudinal study of cognition in subjects with Niemann–Pick disease, type C
  51. Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome
  52. Subclinical seizures in children diagnosed with localization-related epilepsy: Clinical and EEG characteristics
  53. Spiral analysis in Niemann-Pick disease type C
  54. Limbic encephalitis associated with anti-GAD antibody and common variable immune deficiency
  55. IGF system in children with congenital disorders of glycosylation
  56. The long-term outcomes of presymptomatic infants transplanted for Krabbe disease: Report of the workshop held on July 11 and 12, 2008, Holiday Valley, New York
  57. 98. Small molecule therapies for neurologic manifestations of LSD in humans
  58. 99. Long-term clinical trial with miglustat in Niemann-Pick disease type C
  59. 101. Longitudinal study of cognition in subjects with Niemann-Pick disease, type C
  60. 154. Disease stability in patients with Niemann–Pick disease type C treated with miglustat
  61. 100. A multicentre retrospective survey of miglustat in patients with Niemann-Pick type C disease
  62. Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C
  63. The frequency of non-epileptic spells in children: Results of video–EEG monitoring in a tertiary care center
  64. 111. Miglustat in Niemann-Pick disease type C (NPC)
  65. 115. Disease progression in Niemann-Pick disease, type C: Longitudinal
  66. 21 Miglustat in Niemann–Pick type C (NPC) disease: Results of 12-months_ treatment
  67. 71 Niemann-Pick disease, type C: A model for pathophysiology and management of LSDs
  68. WITHDRAWN: 96 Miglustat in Niemann-Pick type C (NPC) disease: Results of 12-months treatment
  69. Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study
  70. Section Editors
  71. Manuel Rodriguez Gomez, MD
  72. Pompe disease diagnosis and management guideline
  73. NPC - LINKS TO DYSLIPIDEMIA BUT NOT CARDIOVASCULAR RISK
  74. Introduction
  75. Metabolic Mimics: The Disorders of N-Linked Glycosylation
  76. The pathophysiology and mechanisms of NP-C disease
  77. Therapy of Niemann–Pick disease, type C
  78. A Riddle Wrapped in a Mystery: Understanding Niemann-Pick Disease, Type C
  79. Identification of 58 novel mutations in Niemann-Pick disease type C: Correlation with biochemical phenotype and importance ofPTC1-like domains inNPC1
  80. Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene
  81. Fabry's Disease
  82. Gangliosidoses
  83. Gaucher's Disease
  84. Hexosaminidase Deficiency
  85. Krabbe's Disease
  86. Leukodystrophy
  87. Leukoencephalopathy
  88. Lipidoses
  89. Abetalipoproteinemia (ABL, Bassen–Kornzweig Disease)
  90. Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia
  91. Niemann-Pick C Variant Detection by Altered Sphingolipid Trafficking and Correlation with Mutations within a Specific Domain of NPC1
  92. Violent recurrent ballism associated with infections in two children with static encephalopathy
  93. Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)
  94. Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome
  95. Mutation causing congenital myasthenia reveals acetylcholine receptor β/δ subunit interaction essential for assembly
  96. Broad screening test for sphingolipid-storage diseases
  97. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion
  98. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion
  99. Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease
  100. Severe Hajdu‐Cheney syndrome with upper airway obstruction
  101. Severe Hajdu-Cheney syndrome with upper airway obstruction
  102. Movement and Allied Disorders in Childhood
  103. Angelman's syndrome: clinical and electroencephalographic findings
  104. Successful Treatment of Intrathecal Methotrexate Overdose by Using Ventriculolumbar Perfusion and Intrathecal Instillation of Carboxypeptidase G2
  105. Childhood Dural Arteriovenous Fistulae of the Posterior Dural Sinuses
  106. Childhood Dural Arteriovenous Fistulae of the Posterior Dural Sinuses
  107. Demyelination in niemann-pick disease, type C
  108. Diagnosis of Niemann-Pick disease type C
  109. Rearrangement of Valproate Glucuronide in a Patient with Drug-Associated Hepatobiliary and Renal Dysfunction
  110. A phase I/II randomised control study of OGT 918 in patients with Niemann-Pick type C disease