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Alcohol and Alcoholism (Oxford, Oxfordshire). Supplement|January 1, 1994
Detection of relapses in alcohol dependent patients using serum carbohydrate deficient transferrin: improvement with individualized reference levelsS Borg, A V Carlsson, A Helander, et al.
Neurology|November 5, 2010
Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblingsB Wandschneider, U A Kopp, M Kliegel, et al.
Pediatria Polska|July 1, 1996
[Jaeken's (CDG) syndrome in two sisters]A T Midro, F Hanefeld, B Zadrozna-Tołwińska, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 15, 1998
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1AS Kjaergaard, B Kristiansson, H Stibler, et al.
Neurobehavioral Toxicology and Teratology|July 1, 1984
Ethanol in preweanling rats with dams: body temperature unaffectedT W Kruckeberg, P K Gaetano, E M Burns, et al.
Neuropediatrics|August 1, 1983
Cranial computed tomography of 64 children in continuous complete remission of leukemia II: relations to patient data and neurological complicationsU Stephani, G Harten, H J Langermann, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 3, 2001
Holoprosencephaly and low molecular weight proteinuria: the human homologue of murine megalin deficiencyD Müller, T Ankermann, U Stephani, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Genomics|February 1, 1997
Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian familiesC Bjursell, H Stibler, J Wahlström, et al.
Archives of Disease in Childhood|March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndromeM Pineda, C Pavia, M A Vilaseca, et al.
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