Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Veysel Nijat Baş"'
Publikováno v:
Korean Journal of Pediatrics, Vol 58, Iss 7, Pp 270-273 (2015)
Legg-Calve-Perthes (LCP) disease is characterized by idiopathic avascular osteonecrosis of the epiphysis of the femur head. The main factor that plays a role in the etiology of the disease is decreased blood flow to the epiphysis. Many predisposing f
Externí odkaz:
https://doaj.org/article/818ad9eb0c7945e882ddc8ed875fee1e
Publikováno v:
Güncel Pediatri. 20:202-208
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766f31c52417c28fbc0f7a063061897d
https://doi.org/10.4274/jcp.2022.90022
https://doi.org/10.4274/jcp.2022.90022
Autor:
Veysel Nijat Baş, Zehra Aycan
Publikováno v:
Volume: 1, Issue: 1 6-11
Archives of Current Medical Research
Archives of Current Medical Research
Childhood obesity prevalence is increasing worldwide. The most common cause of obesity in children is a positive energy balance due to excess caloric intake in contrast to caloric expenditure combined with a genetic predisposition for weight gain. Ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ebe13ac8df3820b0c3b0b15677820c
https://doi.org/10.47482/acmr.2020.1
https://doi.org/10.47482/acmr.2020.1
Autor:
Gonca Kılıç Yıldırım, Veysel Nijat Baş
Publikováno v:
OSMANGAZİ JOURNAL OF MEDICINE.
Phenylketonuria (PKU) is one of the most common preventable causes of intellectual disability resulting from deficiency of phenylalanine hydroxylase enzyme activity. Precocious puberty (PP) is characterized by premature breast and pubic hair developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45fe19120a784d7e2381eeac9a47bb71
https://doi.org/10.20515/otd.675301
https://doi.org/10.20515/otd.675301
Autor:
Sibel Yel, Ruhan Düşünsel, Veysel Nijat Baş, Deniz Okdemir, Nihal Hatipoglu, Zübeyde Gündüz, Kenan Yilmaz, Ismail Dursun
Publikováno v:
Annals of Medical Research. 28:1302
Aim: Thyroid hormones have various effects on kidney function and both hypothyroidism and hyperthyroidism may result in clinicallyimportant alterations in kidney function. Therefore, we evaluated kidney functions and changes in kidney functions over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96e939b61a4a28ca9c23d76488c88a51
https://doi.org/10.5455/annalsmedres.2020.05.467
https://doi.org/10.5455/annalsmedres.2020.05.467
Publikováno v:
Annals of Medical Research. 28:1795
Aim: This study examines the distribution of genital abnormalities based on physical examination of our patients with 46, XY disorders of sex development (46, XY DSD), and aims to define severity and frequency of hypospadias in 46, XY DSD. Hypospadia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc34a5da7e7655f1c25218113a7f983
https://doi.org/10.5455/annalsmedres.2020.08.799
https://doi.org/10.5455/annalsmedres.2020.08.799
Autor:
Meltem Cerrah Gunes, Ozgur Kirbiyik, Ferda Ozkinay, Ayca Aykut, Tahir Atik, Filiz Hazan, Hüseyin Onay, Aslı Ece Solmaz, Veysel Nijat Baş, Ozge Ozalp Yuregir
Publikováno v:
European Journal of Medical Genetics. 58:689-694
WOS: 000366093100010
PubMed ID: 26518167
Bardet-Biedl Syndrome (BBS) is a rare, autosomal-recessive ciliopathy characterized by obesity, rod-cone dystrophy, postaxial polydactyly, renal abnormalities, genital abnormalities and learning diff
PubMed ID: 26518167
Bardet-Biedl Syndrome (BBS) is a rare, autosomal-recessive ciliopathy characterized by obesity, rod-cone dystrophy, postaxial polydactyly, renal abnormalities, genital abnormalities and learning diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fff38e6e74967218709cb39016304adf
https://doi.org/10.1016/j.ejmg.2015.10.011
https://doi.org/10.1016/j.ejmg.2015.10.011
Autor:
Hulya Nalcacioglu, Sibel Yel, Hasan Çetinkaya, Veysel Nijat Baş, Funda Bastug, Binnaz Tekatlı-Çelik
Publikováno v:
The Turkish journal of pediatrics. 60(2)
Bastug F, Nalcacioglu H, Bas VN, Tekatli-Celik B, Cetinkaya H, Yel S. Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome. Turk J Pediatr 2018; 60: 210-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac7fb8e69128238df4cb546a14d9b259
https://pubmed.ncbi.nlm.nih.gov/30325132
https://pubmed.ncbi.nlm.nih.gov/30325132
Publikováno v:
Pediatric emergency care. 35(11)
Objectives L-Thyroxine ingestion is rarely seen in children; here, we report our experience of it. This study describes the clinical characteristics and laboratory findings of acute L-thyroxine ingestion in children. Methods This retrospective study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cd6ff9bb0bfdede34b72d49dbc1843
https://pubmed.ncbi.nlm.nih.gov/28419021
https://pubmed.ncbi.nlm.nih.gov/28419021
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 30
Background:Impaired heart functions in newborns with hypothyroidism should be reversed by levothyroxine substitution therapy. The aim of the study was to investigate heart functions with congenital hypothroidism (CH) in newborns and changes after lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a9a46655f8d92a820ab6db0af99167
https://doi.org/10.1515/jpem-2016-0393
https://doi.org/10.1515/jpem-2016-0393