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Pediatrics

Citations 21-30 of 49 total displayed.

Past content (since Jan 1998):

Neurological Reviews
Progress in Periventricular Leukomalacia
Wenbin Deng; Jeanette Pleasure; David Pleasure
Arch Neurol 2008; 65: 1291-1295. [Abstract] [Full text] [PDF]  

Observations
Myoclonus-Dystonia Due to Maternal Uniparental Disomy
Émilie Guettard; Marie-France Portnoi; Katja Lohmann-Hedrich; Boris Keren; Sylvie Rossignol; Susen Winkler; Imen El Kamel; Smaranda Leu; Emmanuelle Apartis; Marie Vidailhet; Christine Klein; Emmanuel Roze
Arch Neurol 2008; 65: 1380-1385. [Abstract] [Full text] [PDF]  

Original Contributions
Embryonic Myosin Heavy-Chain Mutations Cause Distal Arthrogryposis and Developmental Myosin Myopathy That Persists Postnatally
Homa Tajsharghi; Eva Kimber; Anna-Karin Kroksmark; Ragnar Jerre; Mar Tulinius; Anders Oldfors
Arch Neurol 2008; 65: 1083-1090. [Abstract] [Full text] [PDF]  

Original Contributions
Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome: Novel MPV17 Mutations
Antonella Spinazzola; René Santer; Orhan H. Akman; Kostas Tsiakas; Hansjoerg Schaefer; Xiaoqi Ding; Charalampos L. Karadimas; Sara Shanske; Jaya Ganesh; Salvatore Di Mauro; Massimo Zeviani
Arch Neurol 2008; 65: 1108-1113. [Abstract] [Full text] [PDF]  

Correspondence
Multiple Sclerosis and Recurrent Disseminated Encephalomyelitis Are Different Diseases—Reply
Jérôme de Seze
Arch Neurol 2008; 65: 674-a-675-a. [Extract] [Full text] [PDF]  

Correspondence
Multiple Sclerosis and Recurrent Disseminated Encephalomyelitis Are Different Diseases
Charles M. Poser
Arch Neurol 2008; 65: 674. [Extract] [Full text] [PDF]  

Original Contributions
Cryptogenic Epileptic Syndromes Related to SCN1A: Twelve Novel Mutations Identified
Claudio Zucca; Francesca Redaelli; Roberta Epifanio; Nicoletta Zanotta; Antonino Romeo; Monica Lodi; Pierangelo Veggiotti; Giovanni Airoldi; Chris Panzeri; Romina Romaniello; Gianni De Polo; Paolo Bonanni; Simonetta Cardinali; Cinzia Baschirotto; Loreto Martorell; Renato Borgatti; Nereo Bresolin; Maria Teresa Bassi
Arch Neurol 2008; 65: 489-494. [Abstract] [Full text] [PDF]  

Original Contributions
Cortical Brain Malformations: Effect of Clinical, Neuroradiological, and Modern Genetic Classification
Marie Claire Yvette de Wit; Maarten H. Lequin; Ireneaus F. M. de Coo; Esther Brusse; Dicky J. J. Halley; Raoul van de Graaf; Rachel Schot; Frans W. Verheijen; Grazia M. S. Mancini
Arch Neurol 2008; 65: 358-366. [Abstract] [Full text] [PDF]  

Original Contributions
Long-term Follow-up of Taiwanese Chinese Patients Treated Early for 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
Kai-Ming Liu; Tze-Tze Liu; Ni-Chung Lee; Ling-Yee Cheng; Kwang-Jen Hsiao; Dau-Ming Niu
Arch Neurol 2008; 65: 387-392. [Abstract] [Full text] [PDF]  

Corrections
Error in Figure in: The New Neurobiology of Autism: Cortex, Connectivity, and Neuronal Organization
Arch Neurol 2007; 64: 1464. [Full text] [PDF]  

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