Literature DB >> 21009925

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R HEGGLIN.   

Abstract

Keywords:  LEUKOCYTES

Mesh：

Year:  1945        PMID： 21009925

Source DB:  PubMed          Journal:  Helv Med Acta        ISSN： 0018-0203


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  14 in total

1.  The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Authors:  J A Martignetti; K E Heath; J Harris; N Bizzaro; A Savoia; C L Balduini; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

Review 2.  Genetic abnormalities of Bernard-Soulier syndrome.

Authors:  Shinji Kunishima; Tadashi Kamiya; Hidehiko Saito
Journal:  Int J Hematol       Date:  2002-11       Impact factor: 2.490

3.  May-Hegglin anomaly: a rare cause of thrombocytopenia.

Authors:  A Greinacher; J Bux; V Kiefel; J G White; C Mueller-Eckhardt
Journal:  Eur J Pediatr       Date:  1992-09       Impact factor: 3.183

4.  Glycoprotein Ib is homogeneously distributed on external and internal membranes of resting platelets.

Authors:  J G White; M D Krumwiede; G Escolar
Journal:  Am J Pathol       Date:  1999-12       Impact factor: 4.307

5.  A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.

Authors:  Moon Ju Jang; Hyun-Jeong Park; So Young Chong; Ji Young Huh; In-Ho Kim; Ja-Hyun Jang; Hee-Jin Kim; Doyeun Oh
Journal:  Yonsei Med J       Date:  2012-05       Impact factor: 2.759

6.  Anaesthesia for caesarean delivery in a patient with May-Hegglin anomaly.

Authors:  D M Kotelko
Journal:  Can J Anaesth       Date:  1989-05       Impact factor: 5.063

7.  Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13.

Authors:  A Toren; N Amariglio; G Rozenfeld-Granot; A J Simon; F Brok-Simoni; E Pras; G Rechavi
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

8.  Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

Authors:  K E Heath; A Campos-Barros; A Toren; G Rozenfeld-Granot; L E Carlsson; J Savige; J C Denison; M C Gregory; J G White; D F Barker; A Greinacher; C J Epstein; M J Glucksman; J A Martignetti
Journal:  Am J Hum Genet       Date:  2001-10-04       Impact factor: 11.025

9.  MYH-9 Related Platelet Disorders: Strategies for Management and Diagnosis.

Authors:  Karina Althaus; Andreas Greinacher
Journal:  Transfus Med Hemother       Date:  2010-09-15       Impact factor: 3.747

10.  Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions.

Authors:  A Greinacher; H K Nieuwenhuis; J G White
Journal:  Blut       Date:  1990-11
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