HARLEQUIN ICTHYOSIS: A RARE CASE REPORT Journal title: International Journal of Medical Research & Health Sciences (IJMRHS) Authors: Pradipprava Paria| Dept of pediatrics, R G Kar Medical College, West Bengal University of Health Sci... Subject(s): Medicine, Biomedicine, Dentistry and Oral Surgery, Oncology, Public Health and Community Medicine
Identyfikacja mutacji w mitochondrialnym genie 12S rRNA u osób z niedosłuchem po leczeniu antybiotykami aminoglikozydowymi Journal title: Otolaryngologia Polska Authors: Małgorzata Rydzanicz Subject(s):
Mutational screening of the mitochondrial 12S rRNA gene in Polish patients with aminoglycoside-induced hearing Ioss Journal title: Otolaryngologia Polska Authors: Małgorzata Rydzanicz Subject(s):
Role of molecular examinations in qualification to first line treatment with erlotinib in NSCLC patients based on EURTAC study results Journal title: OncoReview Authors: Paweł Krawczyk Subject(s): Medicine, Cardiology, Internal Medicine, Oncology, Cardiac & Cardiovascular Systems
Znaczenie badań molekularnych w kwalifikacji do terapii I linii erlotynibem chorych na NDRP na podstawie wyników badania EURTAC Journal title: OncoReview Authors: Paweł Krawczyk Subject(s): Medicine, Cardiology, Internal Medicine, Oncology, Cardiac & Cardiovascular Systems
Ocena przebiegu klinicznego przewlekłego zapalenia trzustki u dzieci ze współwystępowaniem mutacji w genach SPINK1 i CFTR Journal title: Postępy Nauk Medycznych Authors: Karolina Wejnarska, Jarosław Kierkuś, Elwira Kołodziejczyk, Józef Ryżko, Grzegorz Oracz Subject(s):
The clinical course of chronic pancreatitis in children with the coincidence of mutations in the CFTR and SPINK1 genes Journal title: Postępy Nauk Medycznych Authors: Karolina Wejnarska, Jarosław Kierkuś, Elwira Kołodziejczyk, Józef Ryżko, Grzegorz Oracz Subject(s):
Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Maciej Miliński, Ewa Buszman, Dorota Wrześniok, Artur Beberok Subject(s): Medicine
Hipomelanocytozy dziedziczne: rola genów PAX3, SOX10, MITF, SNAI2, KIT, EDN3 i EDNRB Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Maciej Miliński, Ewa Buszman, Dorota Wrześniok, Artur Beberok Subject(s): Medicine
Hipomelanozy przekazywane z pokolenia na pokolenie Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Ewa Buszman, Maciej Miliński, Dorota Wrześniok Subject(s): Medicine
Hypomelanoses transmitted from generation to generation Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Ewa Buszman, Maciej Miliński, Dorota Wrześniok Subject(s): Medicine
Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia Journal title: Annals of Hepatology Authors: Mehri Sani, Mozhgan Sabbaghian, Fatemeh Mahjoob, Angelo Cefalù, Maurizio Averna, Nima Rezaei Subject(s):
Impact of Genetically Predisposed Skin Barrier Function Abnormalities on the Onset and Course of Food Allergy in Children Journal title: Здоров`я дитини Authors: O.P. Pakholchuk Subject(s):
Relationship Among Clinical, Laboratory Findings, Disease Severity Scores and Genetic Mutations in Patient with Familial Mediterranean Fever Journal title: HASEKİ TIP BÜLTENİ Authors: Selda Yavuz, Nilgün Selçuk Duru, Murat Elevli Subject(s):
Updates on the Molecular Genetics of Colorectal Cancer Journal title: Colorectal Cancer: Open Access Authors: Katherine Wong, Guofeng Xie Subject(s):
