Results 191 to 200 of about 3,635 (200)

Perioperative management of MYH9 hereditary macrothrombocytopenia (Fechtner syndrome)

European Journal of Haematology, 2007
Kathleen Selleng, Andreas Greinacher, Theodore E Warkentin   +2 more
exaly  

Hereditary Macrothrombocytopenia

Anskar Y.H. Leung, Edmond S.K. Ma
openaire   +1 more source

Demonstration of novel gain‐of‐function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia‐like phenotype

Molecular Genetics & Genomic Medicine, 2013
Hirokazu Kashiwagi, Shinji Kunishima, Kazunobu Kiyomizu   +2 more
exaly  

[MYH9-related macrothrombocytopenia].

La Revue du praticien, 2014
Thomas, Nivet, Delphine, Gobert, Arsène, Mekinian, Tewfik, Bibi-Triki, Olivier, Fain   +4 more
openaire   +1 more source

Progressive macrothrombocytopenia and hearing loss in a large family with DIAPH1 related disease

American Journal of Medical Genetics, Part A, 2017
Akira Ganaha, Tadashi Kaname, Yasutsugu Chinen   +2 more
exaly  

Macrothrombocytopenia: Investigating the Ultrastructure of Platelets and Fibrin Networks Using Scanning and Transmission Electron Microscopy

Ultrastructural Pathology, 2009
Etheresia Pretorius, Hester M Oberholzer, Wendy J van der Spuy   +2 more
exaly  

[Macrothrombocytopenia].

Ryoikibetsu shokogun shirizu, 1997
openaire   +1 more source

ACTN1 rod domain mutation associated with congenital macrothrombocytopenia

Annals of Hematology, 2015
Motoko Yasutomi, Shinji Kunishima, Shintaro Okazaki   +2 more
exaly  

The Role of Microscopy in the Classification of Macrothrombocytopenia

Microscopy and Microanalysis, 2005
openaire   +1 more source

Peripheral Smear In The Diagnosis Of Macrothrombocytopenia

The Internet Journal of Laboratory Medicine, 2011
openaire   +1 more source