Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Avni KAYA"'
Publikováno v:
Medicine Science, Vol 6, Iss 3, Pp 496-7 (2017)
Vitamin B12 (B12) deficiency is associated with growth retardation, reduced serum osteocalcin levels, lower bone mineral density, and increased bone fracture risk, yet the underlying mechanisms remain unclear. However, a recent study showed that B12
Externí odkaz:
https://doaj.org/article/6327889b640d4210a6eb4eedf5013814
Autor:
Sevil ArıYuca, Cahide Yılmaz, Avni Kaya, Lokman Üstyol, Ertan Sal, Yasar Cesur, Hüseyin Caksen
Publikováno v:
Journal of Acute Disease, Vol 3, Iss 1, Pp 74-76 (2014)
The central nervous system is one of the most crucial targeted systems of hyphotiroidism where tissues undergo various broad developmental processes such as neuronal and glial cellular differentiation, migration and myelinization. However brain image
Externí odkaz:
https://doaj.org/article/ba88393801214b60b3442369effbe104
Autor:
Muhammed Akıl, Avni Kaya, M. Selçuk Bektaş, Fesih Aktar, Sinan Akbayram, Salim Bilici, Mehmet Beyazal
Publikováno v:
Journal of Acute Disease, Vol 2, Iss 2, Pp 159-160 (2013)
A 8-year-old boy admitted with abdominal pain, fever and vomiting for the previous 10 days. Sensitivity was detected in the epigastric area. There was not defense and rebond. Aspartate aminotransferase was 106 U/L, alanine aminotransferase 25 U/L, al
Externí odkaz:
https://doaj.org/article/1eb2901c6f864422b68ff11bdb7495d2
Autor:
Avni Kaya, Sevil Ari Yuca, Kamuran Karaman, Remzi Erten, Murat Dogan, Mehmet Selcuk Bektas, Lokman Ustyol
Publikováno v:
Indian Journal of Dermatology, Vol 58, Iss 2, Pp 160-160 (2013)
A 9-day-old male baby was hospitalized after his birth due to some swells under the skin. The hard consistency nodules observed under the skin all over the body of the patient were of different size, and presented lesions, among which the biggest was
Externí odkaz:
https://doaj.org/article/04dca6ff7cf7400db4a6d7bcfdfa53dc
Aim This study aimed to analyze body mass index, estrogen, testosterone, sex-hormone-binding-globulin (SHBG), free androgenic index (FAI), and estrogen/testosterone ratio and their relationship to breast enlargement in newborns. Additionally, we defi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe5d1cc9cc69218ce955038e9c91891c
https://doi.org/10.21203/rs.3.rs-1255844/v1
https://doi.org/10.21203/rs.3.rs-1255844/v1
Autor:
Belma Haliloglu, Avni Kaya, Mehmet Nuri Ozbek, Heybet Tüzün, Sarah E. Flanagan, Muhittin Çelik, Sian Ellard
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Sirolimus has been reported to be effective in the treatment of the diffuse form of congenital hyperinsulinism (CHI), unresponsive to diazoxide and octreotide, without causing severe side effects. Two newborns with CHI due to homozygous ABCC8 gene mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45700c14d4860d85fe841602bd5fcc1
http://europepmc.org/articles/PMC6083472
http://europepmc.org/articles/PMC6083472
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Kisspeptin levels have been reported in children with premature thelarche, precocious puberty and adolescent gynecomastia, but there are no reports on kisspeptin levels in the neonatal period. This study aimed to investigate plasma kisspep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96623386e0803664c5056197a7ce5bf
https://doi.org/10.4274/jcrpe.1994
https://doi.org/10.4274/jcrpe.1994
Publikováno v:
Journal of Pediatric Infectious Diseases. :165-168
Varicella remains a dangerous viral pathogen for pediatric cancer patients. The incidence of primary varicella infection in Eastern of Turkiye is still high because of low vaccination rate. Medical records of 27 pediatric patients with hematological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0142f042b87c64a7cb7c86c79ec3f691
https://doi.org/10.1055/s-0035-1557082
https://doi.org/10.1055/s-0035-1557082
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome is an autosomal dominant genetic disorder characterized by hypoparathyroidism, sensorineural deafness and renal dysplasia. We herein present the first Turkish patient with HDR syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::684a9ec79dd6d788041668c2f298e681
http://europepmc.org/articles/PMC4563186
http://europepmc.org/articles/PMC4563186
Publikováno v:
Journal of Infectious Diseases and Therapeutics. 3:21-25
Purpose : Hyperbilirubinemia is a simple problem for newborn babies, but a very widespread one. Jaundice is seen in the first week of life in 60% of mature babies and in 80% of premature babies. In this study, it is aimed to research hyperbilirubinem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7c693c9224a69606eb7cc4962c081c2
https://doi.org/10.14205/2310-9386.2015.03.01.3
https://doi.org/10.14205/2310-9386.2015.03.01.3