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Frontiers in Endocrinology
|
April 19, 2013
PROK2/PROKR2 Signaling and Kallmann Syndrome
Catherine Dodé, Philippe Rondard
Medecine Sciences : M/S
|
September 14, 2004
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?]
Catherine Dodé, Jean-Pierre Hardelin
Journal of Molecular Medicine (Berlin, Germany)
|
September 15, 2004
Kallmann syndrome: fibroblast growth factor signaling insufficiency?
Catherine Dodé, Jean-Pierre Hardelin
European Journal of Human Genetics : EJHG
|
November 6, 2008
Kallmann syndrome
Catherine Dodé, Jean-Pierre Hardelin
Frontiers of Hormone Research
|
April 15, 2010
Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations
Julie Sarfati, Catherine Dodé, Jacques Young
La Revue Du Praticien
|
March 28, 2002
[Hereditary intermittent fevers, other than familial Mediterranean fevers]
Gilles Grateau, Laurence Cuisset, Catherine Dodé, et al.
Journal of Nephrology
|
July 2, 2003
TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis
Catherine Dodé, Laurence Cuisset, Marc Delpech, et al.
Digestive Diseases and Sciences
|
July 26, 2006
Intestinal pseudo-obstruction as a manifestation of tumor necrosis factor receptor-associated periodic syndrome
Isabelle Marie, Fabien Hervé, Catherine Dodé, et al.
Clinical and Experimental Rheumatology
|
January 31, 2017
Digenic MEFV/TNFRSF1A autoinflammatory syndrome with relapsing aseptic neutrophilic meningitis and chronic myelitis
Anne Murarasu, Catherine Dodé, Guillaume Sarrabay, et al.
Presse Medicale (Paris, France : 1983)
|
November 4, 2004
[Hereditary intermittant fever]
Gilles Grateau, Brigitte Granel, Véronique Hentgen, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Frontiers in Endocrinology
|
April 19, 2013
PROK2/PROKR2 Signaling and Kallmann Syndrome
Catherine Dodé, Philippe Rondard
Medecine Sciences : M/S
|
September 14, 2004
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?]
Catherine Dodé, Jean-Pierre Hardelin
Journal of Molecular Medicine (Berlin, Germany)
|
September 15, 2004
Kallmann syndrome: fibroblast growth factor signaling insufficiency?
Catherine Dodé, Jean-Pierre Hardelin
European Journal of Human Genetics : EJHG
|
November 6, 2008
Kallmann syndrome
Catherine Dodé, Jean-Pierre Hardelin
Frontiers of Hormone Research
|
April 15, 2010
Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations
Julie Sarfati, Catherine Dodé, Jacques Young
La Revue Du Praticien
|
March 28, 2002
[Hereditary intermittent fevers, other than familial Mediterranean fevers]
Gilles Grateau, Laurence Cuisset, Catherine Dodé, et al.
Journal of Nephrology
|
July 2, 2003
TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis
Catherine Dodé, Laurence Cuisset, Marc Delpech, et al.
Digestive Diseases and Sciences
|
July 26, 2006
Intestinal pseudo-obstruction as a manifestation of tumor necrosis factor receptor-associated periodic syndrome
Isabelle Marie, Fabien Hervé, Catherine Dodé, et al.
Clinical and Experimental Rheumatology
|
January 31, 2017
Digenic MEFV/TNFRSF1A autoinflammatory syndrome with relapsing aseptic neutrophilic meningitis and chronic myelitis
Anne Murarasu, Catherine Dodé, Guillaume Sarrabay, et al.
Presse Medicale (Paris, France : 1983)
|
November 4, 2004
[Hereditary intermittant fever]
Gilles Grateau, Brigitte Granel, Véronique Hentgen, et al.
Page
of 5