Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Omer Tarim"'
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Kenny-Caffey syndrome (KCS) is a rare autosomal recessive/dominant disease characterized by hypoparathyroidism, skeletal dysplasia, dwarfism, and dysmorphism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54e8c58b43926721327eeef2692e51c0
https://pubmed.ncbi.nlm.nih.gov/34382758
https://pubmed.ncbi.nlm.nih.gov/34382758
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 97-102 (2023)
Kenny-Caffey syndrome (KCS) is a rare autosomal recessive (AR)/dominant disease characterized by hypoparathyroidism, skeletal dysplasia, dwarfism, and dysmorphism. FAM111A or TBCE gene mutations are responsible for this syndrome. Osteocraniostenosis
Externí odkaz:
https://doaj.org/article/6b07ae1b62fb477b8b7927d90a0a7823
Publikováno v:
Journal of the American College of Nutrition. 16:159-165
Suboptimal nutrition leads to growth delay, frequently without over clinical or biochemical signs. We hypothesize that changes in serum IFG-1 and erythrocyte sodium-potassium ATPase activity (ENKA) may be indices of suboptimal nutrition.Male Sprague-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fb4d4a7307f80756e464edfabb59d59
https://doi.org/10.1080/07315724.1997.10718667
https://doi.org/10.1080/07315724.1997.10718667
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 57(5)
The aim of this retrospective study was to investigate pheochromocytoma (pheo), which is a rare endocrine tumor in the pediatric population.The medical records of five children with pheo were studied. The age, gender, clinical presentation, family hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::37d3268c895c60da9b04ddc7e67b2af7
https://pubmed.ncbi.nlm.nih.gov/25916248
https://pubmed.ncbi.nlm.nih.gov/25916248
Autor:
Fima Lifshitz, Omer Tarim
Publikováno v:
The Journal of Nutrition. 126:1031S-1041S
Expert panels recommend reduction of dietary fat and cholesterol, because excessive fat intake may lead to known health hazards. However, there are no data demonstrating beneficial effects of such diets starting in childhood for all children, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938477eb60f2e72c90c875e6d2a3d1a8
https://doi.org/10.1093/jn/126.suppl_4.1031s
https://doi.org/10.1093/jn/126.suppl_4.1031s
Publikováno v:
Endocrinology and Metabolism Clinics of North America. 22:673-683
Adolescence is often considered a nutritionally vulnerable period because of its characteristic rapid physical and psychological changes. Nutritional risks for both undernutrition and overnutrition are present and may be increased during physiologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4208ae9312b4045db49af8618f43f82f
https://doi.org/10.1016/s0889-8529(18)30157-9
https://doi.org/10.1016/s0889-8529(18)30157-9
Autor:
Yasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, Elif Sobu, Sian Ellard, Elisa De Franco, Ömer Tarım
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 80-87 (2021)
Objective:Neonatal diabetes mellitus (NDM) may be transient or permanent, and the majority is caused by genetic mutations. Early diagnosis is essential to select the patients who will respond to oral treatment. In this investigation, we aimed to pres
Externí odkaz:
https://doaj.org/article/7581c28c44f94a79bac473eee704e61d
Autor:
Zeynep Şıklar, Serap Turan, Abdullah Bereket, Firdevs Baş, Tülay Güran, Azad Akberzade, Ayhan Abacı, Korcan Demir, Ece Böber, Mehmet Nuri Özbek, Cengiz Kara, Şükran Poyrazoğlu, Murat Aydın, Aslı Kardelen, Ömer Tarım, Erdal Eren, Nihal Hatipoğlu, Muammer Büyükinan, Nesibe Akyürek, Semra Çetinkaya, Elvan Bayramoğlu, Beray Selver Eklioğlu, Ahmet Uçaktürk, Saygın Abalı, Damla Gökşen, Yılmaz Kor, Edip Ünal, İhsan Esen, Ruken Yıldırım, Onur Akın, Atilla Çayır, Emine Dilek, Birgül Kırel, Ahmet Anık, Gönül Çatlı, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 12, Iss 2, Pp 150-159 (2020)
Objective:Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options.Methods:Here w
Externí odkaz:
https://doaj.org/article/57157ae9f20b435fb128022ec51d0c16
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 41(4)
The relationship between hemoglobin A1c (HbA1c) and iron status in type 1 diabetes mellitus (DM) has not been adequately studied. In this prospective investigation, we aimed to determine the effect of iron deficiency on HbA1c in diabetic patients who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e6f8fee90042d6668e20b3bfcb799db
https://pubmed.ncbi.nlm.nih.gov/10453183
https://pubmed.ncbi.nlm.nih.gov/10453183