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JIMD Reports
|
February 23, 2013
Successful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome
Anne Laure Sellier, Philippe Labrune, Theresa Kwon, et al.
Presse Medicale (Paris, France : 1983)
|
March 4, 2008
[Natural history of hepatic glycogen storage diseases]
Philippe Labrune, Pascale Trioche Eberschweiler, Alix Mollet Boudjemline, et al.
Journal of Inherited Metabolic Disease
|
November 25, 2010
Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type Ib
Alix Mollet Boudjemline, Arnaud Isapof, Jean-Bernard Witas, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 29, 2005
Recurring acute abdominal pains in an adolescent as the presenting manifestations of hereditary angioneurotic oedema
Laurence Foix-L'Hélias, Laurence Weiss, Alix Mollet-Boudjemline, et al.
Orphanet Journal of Rare Diseases
|
May 24, 2011
Glucose-6-phosphatase deficiency
Roseline Froissart, Monique Piraud, Alix Mollet Boudjemline, et al.
JIMD Reports
|
February 23, 2013
Perioperative management of hemostasis for surgery of benign hepatic adenomas in patients with glycogen storage disease type ia
Alix Mollet-Boudjemline, Aurélie Hubert-Buron, Catherine Boyer-Neumann, et al.
European Journal of Human Genetics : EJHG
|
January 17, 2008
The Tunisian population history through the Crigler-Najjar type I syndrome
François M Petit, Stéphane Bézieau, Vincent Gajdos, et al.
Plos Medicine
|
October 8, 2010
Effectiveness of chest physiotherapy in infants hospitalized with acute bronchiolitis: a multicenter, randomized, controlled trial
Vincent Gajdos, Sandrine Katsahian, Nicole Beydon, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
JIMD Reports
|
February 23, 2013
Successful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome
Anne Laure Sellier, Philippe Labrune, Theresa Kwon, et al.
Presse Medicale (Paris, France : 1983)
|
March 4, 2008
[Natural history of hepatic glycogen storage diseases]
Philippe Labrune, Pascale Trioche Eberschweiler, Alix Mollet Boudjemline, et al.
Journal of Inherited Metabolic Disease
|
November 25, 2010
Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type Ib
Alix Mollet Boudjemline, Arnaud Isapof, Jean-Bernard Witas, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 29, 2005
Recurring acute abdominal pains in an adolescent as the presenting manifestations of hereditary angioneurotic oedema
Laurence Foix-L'Hélias, Laurence Weiss, Alix Mollet-Boudjemline, et al.
Orphanet Journal of Rare Diseases
|
May 24, 2011
Glucose-6-phosphatase deficiency
Roseline Froissart, Monique Piraud, Alix Mollet Boudjemline, et al.
JIMD Reports
|
February 23, 2013
Perioperative management of hemostasis for surgery of benign hepatic adenomas in patients with glycogen storage disease type ia
Alix Mollet-Boudjemline, Aurélie Hubert-Buron, Catherine Boyer-Neumann, et al.
European Journal of Human Genetics : EJHG
|
January 17, 2008
The Tunisian population history through the Crigler-Najjar type I syndrome
François M Petit, Stéphane Bézieau, Vincent Gajdos, et al.
Plos Medicine
|
October 8, 2010
Effectiveness of chest physiotherapy in infants hospitalized with acute bronchiolitis: a multicenter, randomized, controlled trial
Vincent Gajdos, Sandrine Katsahian, Nicole Beydon, et al.
Page
of 1