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Human Genetics
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October 21, 2010
Gene symbol: MAP2K2. Disease: Cardio-Facio-Cutaneous syndrome
Nadine Hanna, Béatrice Parfait
Annales De Biologie Clinique
|
September 13, 2022
Genetic of thoracic aorta aneurysm
Margaux Cadenet, Nadine Hanna, Pauline Arnaud
The Journal of Rheumatology
|
March 3, 2015
A case of rheumatoid arthritis associated with SMAD3 gene mutation: a new clinical entity?
Elise Berthet, Nadine Hanna, Charlotte Giraud, et al.
Medecine Sciences : M/S
|
November 9, 2005
[Mutation mechanisms and their consequences]
Nadine Hanna, Béatrice Parfait, Dominique Vidaud, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
Marfanoid habitus, inguinal hernia, advanced bone age, and distinctive facial features: a new collagenopathy?
André Mégarbané, Nadine Hanna, Eliane Chouery, et al.
Genes
|
February 14, 2019
Reference Expression Profile of Three <i>FBN1</i> Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome
Louise Benarroch, Mélodie Aubart, Marie-Sylvie Gross, et al.
FEBS Letters
|
April 28, 2006
Reduced phosphatase activity of SHP-2 in LEOPARD syndrome: consequences for PI3K binding on Gab1
Nadine Hanna, Alexandra Montagner, Wen Hwa Lee, et al.
Annals of Vascular Surgery
|
August 26, 2021
The natural history of a family with aortic dissection associated with a novel ACTA2 variant
Pascal Delsart, Clémence Vanlerberghe, Francis Juthier, et al.
Genes
|
August 24, 2018
Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression
Louise Benarroch, Mélodie Aubart, Marie-Sylvie Gross, et al.
Human Mutation
|
April 14, 2025
Early-Onset Aortic Dissection: Characterization of a New Pathogenic Splicing Variation in the <i>MYH11</i> Gene with Several In-Frame Abnormal Transcripts
Pauline Arnaud, Margaux Cadenet, Zakaria Mougin, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Human Genetics
|
October 21, 2010
Gene symbol: MAP2K2. Disease: Cardio-Facio-Cutaneous syndrome
Nadine Hanna, Béatrice Parfait
Annales De Biologie Clinique
|
September 13, 2022
Genetic of thoracic aorta aneurysm
Margaux Cadenet, Nadine Hanna, Pauline Arnaud
The Journal of Rheumatology
|
March 3, 2015
A case of rheumatoid arthritis associated with SMAD3 gene mutation: a new clinical entity?
Elise Berthet, Nadine Hanna, Charlotte Giraud, et al.
Medecine Sciences : M/S
|
November 9, 2005
[Mutation mechanisms and their consequences]
Nadine Hanna, Béatrice Parfait, Dominique Vidaud, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
Marfanoid habitus, inguinal hernia, advanced bone age, and distinctive facial features: a new collagenopathy?
André Mégarbané, Nadine Hanna, Eliane Chouery, et al.
Genes
|
February 14, 2019
Reference Expression Profile of Three <i>FBN1</i> Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome
Louise Benarroch, Mélodie Aubart, Marie-Sylvie Gross, et al.
FEBS Letters
|
April 28, 2006
Reduced phosphatase activity of SHP-2 in LEOPARD syndrome: consequences for PI3K binding on Gab1
Nadine Hanna, Alexandra Montagner, Wen Hwa Lee, et al.
Annals of Vascular Surgery
|
August 26, 2021
The natural history of a family with aortic dissection associated with a novel ACTA2 variant
Pascal Delsart, Clémence Vanlerberghe, Francis Juthier, et al.
Genes
|
August 24, 2018
Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression
Louise Benarroch, Mélodie Aubart, Marie-Sylvie Gross, et al.
Human Mutation
|
April 14, 2025
Early-Onset Aortic Dissection: Characterization of a New Pathogenic Splicing Variation in the <i>MYH11</i> Gene with Several In-Frame Abnormal Transcripts
Pauline Arnaud, Margaux Cadenet, Zakaria Mougin, et al.
Page
of 5