Neuropediatrics
Issue 06 · December 1995
Recommend Journal
eFirst
Issue
287
Voit, T.:
Editorial
Full Text
PDF (114 kb)
Original articles
288
Rocchigiani, M.; Sestini, S.; Micheli, V.; Pescaglini, M.; Jacomelli, G.; Hayek, G.; Pompucci, G.:
Purine and Pyridine Nucleotide Metabolism in the Erythrocytes of Patients with Rett Syndrome
Full Text
PDF (577 kb)
293
Vainzof, M.; Marie, S. K. N.; Reed, U. C.; Schwartzman, J. S.; Pavanello, R. C. M.; Passos-Bueno, M. R.; Zatz, M.:
Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter Alterations
Full Text
PDF (888 kb)
298
Shawkat, Fatima S.; Kingsley, D.; Kendall, B.; Russell-Eggitt, Isabelle; Taylor, D. S. I.; Harris, Chr. M.:
Neuroradiological and Eye Movement Correlates in Children with Intermittent Saccade Failure: "Ocular Motor Apraxia"
Full Text
PDF (1156 kb)
Short communications
306
Derex, L.; Isnard, H.; Revol, M.:
Progressive Facial Hemiatrophy with Multiple Benign Tumors and Hamartomas
Full Text
PDF (1296 kb)
310
Brandt, B. Ryde; Rosén, I.:
Impaired Peripheral Somatosensory Function in Children with Down Syndrome
Full Text
PDF (257 kb)
313
Gascon, G. G.; Chavis, P.; Yaghmour, A.; Stigsby, B.; Ozand, P.; Siddique, T.:
Familial Childhood Primary Lateral Sclerosis with Associated Gaze Paresis
Full Text
PDF (1504 kb)
320
Boltshauser, E.; Forster, I.; Deonna, T.; Willi, U.:
Joubert Syndrome: Are Kidneys Involved?
Full Text
PDF (212 kb)
322
Barbot, C.; Martins, E.; Vilarinho, L.; Dorche, C.; Cardoso, M. L.:
A Mild Form of Infantile Isolated Sulphite Oxidase Deficiency
Full Text
PDF (832 kb)
325
Gordon, B. A.; Gordon, K. E.; Seo, H. C.; Yang, M.; DiCioccio, R. A.; O'Brien, J. S.:
Fucosidosis with Dystonia
Full Text
PDF (563 kb)
328
Zammarchi, E.; Donati, M. A.; Ciani, F.:
Transient Neonatal Nonketotic Hyperglycinemia: A 13-Year Follow-Up
Full Text
PDF (300 kb)
331
Boltshauser, E.; Gehrmann, J.; Steinlin, M.; Eich, G.; Spiegel, R.:
Progressive Subcutaneous and Periarticular Calcifications in a Patient with Spinal Muscular Atrophy Type III
Full Text
PDF (721 kb)
Letters to the editor
333
Rees, M.; Elmslie, F.; Whitehouse, W.; Sundqvist, A.; Gardiner, M.:
Analysis of a Human Brain Voltage-Gated Potassium Channel Gene, KCNA6 (HBK2), in Patients with Juvenile Myoclonic Epilepsy
Full Text
PDF (267 kb)
335
Anlar, B.; Kuruoǧlu, R.; Varh, K.; Renda, Y.:
Acetylcholine Receptor Antihodies and Single-Fiber EMG in First-Degree Relatives of Children with Myasthenia Gravis
Full Text
PDF (280 kb)
Most Read
Archive
Free Sample Issue
Journal
Aims and Scope
Editorial Board
German National License
Authors
Instructions for Authors
Submit a Manuscript
Resident & Fellow section
Subscription
Subscription Information & Contacts
Institutional Licensing
Society
Instructions for Authors
Submit a Manuscript
Resident & Fellow section
NPED Women
Instructions for Authors
Submit a Manuscript
Resident & Fellow section
Journals
Book Series
Login
Help
Portal
Return to Classic Website