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Respiration Physiology|January 4, 1998
Intracellular signal pathways controlling respiratory neuronsD W Richter, P M Lalley, O Pierrefiche, et al.
The Journal of Pediatrics|January 1, 1997
Treatment of apneustic respiratory disturbance with a serotonin-receptor agonistB Wilken, P Lalley, A M Bischoff, et al.
Annals of Neurology|August 1, 1996
Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotypeG C Korenke, S Fuchs, E Krasemann, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 3, 2010
Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysisC Stauch, H Reiber, M Rauchenzauner, et al.
Clinical Genetics|January 1, 1988
A new chromosomal instability disorder confirmed by complementation studiesR D Wegner, M Metzger, F Hanefeld, et al.
Neurology|December 13, 2006
High seroprevalence of Epstein-Barr virus in children with multiple sclerosisD Pohl, B Krone, K Rostasy, et al.
Human Genetics|November 3, 1998
Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndromeT Tvrdik, S Marcus, S M Hou, et al.
Annals of Neurology|August 1, 1992
Multiple sclerosis in children: cerebral metabolic alterations monitored by localized proton magnetic resonance spectroscopy in vivoH Bruhn, J Frahm, K D Merboldt, et al.
Pediatric Neurology|September 1, 1996
Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patientsG C Korenke, P J Pouwels, J Frahm, et al.
Journal of the Neurological Sciences|June 10, 1998
Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutationE Wilichowski, G C Korenke, W Ruitenbeek, et al.
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