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B Desprechins

Showing results (41-50 of 44) with videos related to

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Digestive Diseases and Sciences|February 1, 1993
Endoscopic obliteration of recurrent tracheoesophageal fistulaY Vandenplas, R Helven, H Derop, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiencyK M Gibson, R S Wappner, S Jooste, et al.
British Journal of Haematology|August 8, 1998
The use of the anti-malaria drug Fansidar (pyrimethamine and sulphadoxine) in the treatment of a patient with autoimmune lymphoproliferative syndrome and Fas deficiencyJ E van der Werff ten Bosch, C Demanet, N Balduck, et al.
Neurology|March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyriaA C Jansen, A Oostra, B Desprechins, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Digestive Diseases and Sciences|February 1, 1993
Endoscopic obliteration of recurrent tracheoesophageal fistulaY Vandenplas, R Helven, H Derop, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiencyK M Gibson, R S Wappner, S Jooste, et al.
British Journal of Haematology|August 8, 1998
The use of the anti-malaria drug Fansidar (pyrimethamine and sulphadoxine) in the treatment of a patient with autoimmune lymphoproliferative syndrome and Fas deficiencyJ E van der Werff ten Bosch, C Demanet, N Balduck, et al.
Neurology|March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyriaA C Jansen, A Oostra, B Desprechins, et al.
Pageof 5