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Neurology
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Metabolic disease (inherited)

Citations 21-30 of 116 total displayed.

Past content (since Jul 2001):

CLINICAL/SCIENTIFIC NOTES
Absence of cognitive, behavioral, or emotional dysfunction in progressive muscular atrophy
P. Wicks, S. Abrahams, P. N. Leigh, T. Williams, and L. H. Goldstein
Neurology 2006; 67: 1718-1719. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Late-onset multiple acyl-CoA dehydrogenase deficiency: A frequently missed diagnosis?
S. Köppel, J. Gottschalk, G. F. Hoffmann, H. R. Waterham, H. Blobel, and S. Kölker
Neurology 2006; 67: 1519. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Subcortical white matter abnormalities related to drug resistance in Wilson disease
D. Aikath, A. Gupta, I. Chattopadhyay, M. A. Hashmi, P. K. Gangopadhyay, S. K. Das, and K. Ray
Neurology 2006; 67: 878-880. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiency
A. Schulze, G. F. Hoffmann, P. Bachert, S. Kirsch, G. S. Salomons, N. M. Verhoeven, and E. Mayatepek
Neurology 2006; 67: 719-721. [Abstract] [Full text] [PDF]  

ARTICLES
GAMT deficiency: Features, treatment, and outcome in an inborn error of creatine synthesis
S. Mercimek-Mahmutoglu, S. Stoeckler-Ipsiroglu, A. Adami, R. Appleton, H. Caldeira Araújo, M. Duran, R. Ensenauer, E. Fernandez-Alvarez, P. Garcia, C. Grolik, C. B. Item, V. Leuzzi, I. Marquardt, A. Mühl, R. A. Saelke-Kellermann, G. S. Salomons, A. Schulze, R. Surtees, M. S. van der Knaap, R. Vasconcelos, N. M. Verhoeven, L. Vilarinho, E. Wilichowski, and C. Jakobs
Neurology 2006; 67: 480-484. [Abstract] [Full text] [PDF]  

EDITORIALS
Peripheral nerve involvement in Krabbe disease: A guide to therapy selection and evaluation
Hugo W. Moser
Neurology 2006; 67: 201-202. [Full text] [PDF]  

ARTICLES
Peripheral neuropathy in Krabbe disease: Effect of hematopoietic stem cell transplantation
Zaeem A. Siddiqi, Donald B. Sanders, and Janice M. Massey
Neurology 2006; 67: 268-272. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Vitamins and entacapone in levodopa-induced hyperhomocysteinemia: A randomized controlled study
R. B. Postuma, A. J. Espay, C. Zadikoff, O. Suchowersky, W.R.W. Martin, A. -L. Lafontaine, R. Ranawaya, R. Camicioli, and A. E. Lang
Neurology 2006; 66: 1941-1943. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Fixation-sensitive myoclonus in Lafora disease
S. Kumada, M. Kubota, M. Hayashi, A. Uchiyama, K. Kurata, and Y. Kagamihara
Neurology 2006; 66: 1574-1576. [Abstract] [Full text] [PDF]  

ARTICLES
Global and regional volume changes in the brains of patients with phenylketonuria
B. Pérez-Dueñas, J. Pujol, C. Soriano-Mas, H. Ortiz, R. Artuch, M. A. Vilaseca, and J. Campistol
Neurology 2006; 66: 1074-1078. [Abstract] [Full text] [PDF]  

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* Related collections:
 Medical/Systemic disease
 All Medical/Systemic disease
 Electrolyte
 Endocrine
 Gastrointestinal
 Hematologic
 Nutritional
 Hypoglycemia
 Metabolic disease (inherited)
 Amino acid
 Leukodystrophies
 Lipidoses
 Organic acid
 Peroxisomes
 Glycogenoses


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