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Author/Creator Nurden, Alan

1. A novel missense mutation in a leucine‐rich repeat of GPIbα in a Bernard‐Soulier variant reduces shear‐dependent adherence on von Willebrand factor. (1st July 2019)

Authors:
Proulle, Valerie; Strassel, Catherine; Perrault, Christelle; Baas, Marie‐Jeanne; Moog, Sylvie; Mangin, Pierre; Nurden, Paquita; Nurden, Alan; Adam, Frederic; Bryckaert, Marijke; Kauskot, Alexandre; Li, Renhao; Lanza, Francois
Journal:
British journal of haematology
Issue:
Volume 186:Number 6(2019)
Page Start:
e184
Record Type:
Journal Article
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3. Mutation spectrum and genotype‐phenotype correlations in a large French cohort of MYH9‐Related Disorders. Issue 4 (7th February 2014)

Authors:
Saposnik, Béatrice; Binard, Sylvie; Fenneteau, Odile; Nurden, Alan; Nurden, Paquita; Hurtaud‐Roux, Marie‐Françoise; Schlegel, Nicole; the French MYH9 network
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 2:Issue 4(2014:Jul.)
Page Start:
297
Record Type:
Journal Article
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4. Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α‐granules. Issue 2 (17th November 2017)

Authors:
Favier, Marie; Bordet, Jean‐Claude; Favier, Remi; Gkalea, Vasiliki; Pillois, Xavier; Rameau, Philippe; Debili, Najet; Alessi, Marie‐Christine; Nurden, Paquita; Raslova, Hana; Nurden, Alan
Journal:
American journal of hematology
Issue:
Volume 93:Issue 2(2018:Feb.)
Page Start:
195
Record Type:
Journal Article
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5. Spectrum of the Mutations in Bernard–Soulier Syndrome. Issue 9 (15th July 2014)

Authors:
Savoia, Anna; Kunishima, Shinji; De Rocco, Daniela; Zieger, Barbara; Rand, Margaret L.; Pujol‐Moix, Nuria; Caliskan, Umran; Tokgoz, Huseyin; Pecci, Alessandro; Noris, Patrizia; Srivastava, Alok; Ward, Christopher; Morel‐Kopp, Marie‐Christine; Alessi, Marie‐Christine; Bellucci, Sylvia; Beurrier, P...
Journal:
Human mutation
Issue:
Volume 35:Issue 9(2014:Sep.)
Page Start:
1033
Record Type:
Journal Article
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