Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hilal Unsal"'
Autor:
Elif Soyak Aytekin, Umit M. Sahiner, Sevda Tuten Dal, Hilal Unsal, Ozan Hakverdi, Berna Oguz, Yasemin Ozsurekci, Bulent E. Sekerel, Ozge Soyer
Publikováno v:
Pediatric Pulmonology. 57:1668-1676
It is not clear whether asthma, the most frequent chronic disease in childhood, is a risk for severe SARS-CoV-2 infection in the pediatric population and how SARS-CoV-2 infection affects the lung functions in these patients.We aimed to investigate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::185fae31dec92ca18612073bf67e2432
https://doi.org/10.1002/ppul.25949
https://doi.org/10.1002/ppul.25949
Publikováno v:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and ImmunologyREFERENCES. 33(4)
Legumes are nutritionally valuable as an inexpensive protein source, but may cause severe allergic reactions. This study aimed to identify the characteristics of legume allergies (LAs) in Turkish children.A total of 87 children (4.9 (3.1-7.0) years)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f78ddf9c4ae277b0e48a3e0131c87d3
https://pubmed.ncbi.nlm.nih.gov/35470935
https://pubmed.ncbi.nlm.nih.gov/35470935
Autor:
Emine Polat, Fatma Zehra Öztek Çelebi, Melahat Melek Oguz, Saliha Senel, Husniye Yucel, Esma Altinel Acoglu, Gürses Şahin, Hilal Unsal, Meltem Akcaboy, Eyup Sari
Publikováno v:
Pediatric Hematology and Oncology. 36:1-16
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening syndrome of excessive immune activation. Secondary HLH syndrome develops as a complication of infection, drugs, rheumatologic conditions, or malignancy. The main objectives of this work w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca5f6e1d14f3c5498a7b6bbdeac4ebc
https://doi.org/10.1080/08880018.2019.1572253
https://doi.org/10.1080/08880018.2019.1572253
Autor:
Michael Krainer, Kanamaru R, Kurt J. Isselbacher, Daniel A. Haber, Chikashi Ishioka, Michael G. FitzGerald, Akira Shimada, Anne M. Bowcock, Sandra Silva-Arrieta, Hilal Unsal, Dianne M. Finkelstein, Deborah J. MacDonald
Publikováno v:
New England Journal of Medicine. 336:1416-1422
Background Germ-line mutations in the BRCA1 and BRCA2 genes predispose women to breast cancer. BRCA1 mutations are found in approximately 12 percent of women with breast cancer of early onset, and the specific mutation causing a deletion of adenine a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d1c1c04fd6a922c4879e3731bf6ad01
https://doi.org/10.1056/nejm199705153362003
https://doi.org/10.1056/nejm199705153362003
Autor:
Daniel A. Haber, Kathleen A. Mayzel, Peggy Beer-Romero, Dianne M. Finkelstein, Erin O'Neil, Michael Krainer, Kurt J. Isselbacher, Jerry Younger, Stephen H. Friend, Christoph Englert, Hilal Unsal, Dennis C. Sgroi, Rosemary B. Duda, Barbara L. Smith, Michael G. FitzGerald, Deborah J. MacDonald, Ingrid Hoover, Sandra Silva-Arrieto, Judy Garber
Publikováno v:
New England Journal of Medicine. 334:143-149
Background Mutations in a germ-line allele of the BRCA1 gene contribute to the familial breast cancer syndrome. However, the prevalence of these mutations is unknown in women with breast cancer who do not have the features of this familial syndrome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61de75c79a1a0e592f0b7576f5fba055
https://doi.org/10.1056/nejm199601183340302
https://doi.org/10.1056/nejm199601183340302
Autor:
Christophe Marcais, Hans Zentgraf, Hilal Unsal, Cengiz Yakicier, Kurt J. Isselbacher, Martin Volkmann, Michael Kew, Mehmet Ozturk
Publikováno v:
Proceedings of the National Academy of Sciences. 91:822-826
We studied 80 hepatocellular carcinomas from three continents for p53 gene (TP53) mutations and hepatitis B virus (HBV) sequences. p53 mutations were frequent in tumors from Mozambique but not in tumors from South Africa, China, and Germany. Independ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9574fca010b3e2f708885951264d2e82
https://doi.org/10.1073/pnas.91.2.822
https://doi.org/10.1073/pnas.91.2.822
Autor:
Daniel A. Haber, Jonathan F. Bean, Dianne M. Finkelstein, Deborah J. MacDonald, D P Harkin, S R Hegde, Michael G. FitzGerald, Kurt J. Isselbacher, Hilal Unsal
Publikováno v:
Nature genetics. 15(3)
Ataxia telangiectasia (AT) is a recessive syndrome, including cerebellar degeneration, immunologic defects and cancer predisposition, attributed to mutations in the recently isolated ATM (ataxia telangiectasia, mutated) gene. AT is diagnosed in 1/40,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b20de31ab5f5c6b3415d57387fac0a60
https://pubmed.ncbi.nlm.nih.gov/9054927
https://pubmed.ncbi.nlm.nih.gov/9054927