نتایج جستجو برای: hereditary stability

تعداد نتایج: 382625  

Journal: :Archives of Internal Medicine 2001

Journal: :Srpski arhiv za celokupno lekarstvo 2014

Journal: :Deutsches Aerzteblatt Online 2018

Journal: :CONTINUUM: Lifelong Learning in Neurology 2008

Journal: :Journal of Algebra 2016

Journal: :Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons 2010
Benn Larkin Lieberman Michelle K Kennedy Dorothy R Lorenzo Louis J Reed Arthur K Adamo Vito A Cardo Victor M Badner

6. Spaulding WB: Methyltestosterone therapy for hereditary episodic edema (hereditary angioneurotic edema). Ann Intern Med 53:739, 1960 7. Gelfand JA, Sherins RJ, Alling DW, et al: Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities. N Engl J Med 295:1444, 1976 8. Leimbruger A, Jaques WA, Spaeth RJ: Hereditary angioedema uncomplicated maxillofacia...

2005
T Rajkumar N Soumittra E Vidubala V Sridevi V Mahajan SG Ramanan S Vijaya

Hereditary cancers are thought to account for around 5% of cancers, particularly breast/ovarian and colorectal cancers. In India there is a paucity of data on hereditary cancers and the mutations in some of the common genes linked to hereditary cancers, such as BRCA1, BRCA2, hMSH2 and hMLH1. The country's first comprehensive hereditary cancer clinic was established in February 2002. The article...

Thyroid cancer is a malignancy of the thyroid parenchymal cells. There are four main types of thyroid cancer: papillary thyroid cancer (PTC), follicular thyroid cancer (FTC), anaplastic thyroid carcinoma (ATC), and Medullary thyroid carcinoma (MTC). Medullary thyroid cancer (MTC) is a rare neuroendocrine tumor of the thyroid gland derived from parafollicular C-cells that produce calcitonin (CT...

Journal: :Haematologica 2012
Paola Bianchi Elisa Fermo Cristina Vercellati Anna P Marcello Laura Porretti Agostino Cortelezzi Wilma Barcellini Alberto Zanella

BACKGROUND The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly targeting the hereditary spherocytosis molecular defect (eosin-5'-maleimide-binding test) has been proposed. None of the available tests identifies all cases of hereditary spherocytosis. DESIGN AND METHODS We compare...

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