Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pramuk Amarinthnukrowh"'
Autor:
Vorasuk Shotelersuk, Kanya Suphapeetiporn, Supang Maneesri le Grand, Nipan Israsena, Praewphan Ingrungruanglert, Darintr Sosothikul, Pramuk Amarinthnukrowh, Ruttachuk Rungsiwiwut
Publikováno v:
Thrombosis and Haemostasis. 113:792-805
SummaryWiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder characterised by microthrombocytopenia, complex immunodeficiency, autoimmunity, and haematologic malignancies. It is caused by mutations in the gene encoding WAS protein (WASP),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba4119a96bd219def8842d531b3480c9
https://doi.org/10.1160/th14-06-0503
https://doi.org/10.1160/th14-06-0503
Autor:
Darintr Sosothikul, Pramuk Amarinthnukrowh, S. Ittiporn, Pantipa Chatchatee, Kanya Suphapeetiporn, Siraprapa Tongkobpetch, Vorasuk Shotelersuk
Publikováno v:
Scandinavian Journal of Immunology. 77:69-74
Wiskott–Aldrich syndrome (WAS) is an X-linked recessive primary immunodeficiency disorder caused by mutations in the gene encoding the WAS protein (WASP). Classic WAS is characterized by thrombocytopenia with small-sized platelets, recurrent infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36f10b0204cbeeaa65313ebf203b832f
https://doi.org/10.1111/sji.12004
https://doi.org/10.1111/sji.12004
Autor:
Pramuk Amarinthnukrowh, Vorasuk Shotelersuk, Wipa Panmontha, Ponghatai Damrongphol, Tayard Desudchit, Kanya Suphapeetiporn
Publikováno v:
Genetics and Molecular Research. 15
Fucosidosis is a rare lysosomal storage disorder inherited in an autosomal recessive manner. Its estimated frequency is below 1 in 200,000 live births. Its clinical phenotypes include progressive neurological and mental deterioration, coarse facial f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ab6e8847cb691cf37f517b790510a45
https://doi.org/10.4238/gmr.15038733
https://doi.org/10.4238/gmr.15038733
Autor:
P. Martin van Hagen, Narissara Suratannon, Chalurmpon Srichomthong, Pramuk Amarinthnukrowh, Pantipa Chatchatee, Marjolein Wentink, Darintr Sosothikul, Vorasuk Shotelersuk, Kanya Suphapeetiporn, Gertjan J. Driessen, Mirjam van der Burg, Patra Yeetong
Publikováno v:
Pediatric Allergy and Immunology, 27(2), 214-217. Blackwell Publishing
_To the Editor,_ Leukocyte adhesion deficiency (LAD) is a rare primary immunodeficiency disease characterized by impairment of phagocyte adhesion. Three subtypes have been classified by distinct phases of the adhesion cascade. LAD-III is caused by de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cbe704f7805af3f5ba600eb4b5d7733
https://pure.eur.nl/en/publications/64ae3f60-34ce-44ef-8cf0-d12f61b5b0f5
https://pure.eur.nl/en/publications/64ae3f60-34ce-44ef-8cf0-d12f61b5b0f5
Autor:
Pramuk Amarinthnukrowh, Apichai Kongpatanayothin, Kanya Suphapeetiporn, Siraprapa Tongkobpetch, Vorasuk Shotelersuk
Publikováno v:
Genetic testing and molecular biomarkers. 14(6)
to describe genetic features of five unrelated Thai families with infantile-onset Pompe disease caused by mutations in the acid α-glucosidase (GAA) gene.total RNA and genomic DNA were extracted from peripheral blood leukocytes, and mutation analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77dc1843c652c0d1ea2510864af6ad0f
https://pubmed.ncbi.nlm.nih.gov/21039225
https://pubmed.ncbi.nlm.nih.gov/21039225
Autor:
Praewphan Ingrungruanglert, Pramuk Amarinthnukrowh, Ruttachuk Rungsiwiwut, Supang Maneesri-le Grand, Darintr Sosothikul, Kanya Suphapeetiporn, Nipan Israsena, Vorasuk Shotelersuk
Publikováno v:
Thrombosis & Haemostasis; Apr2015, Vol. 113 Issue 4, p792-805, 14p