Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ahmet Midhat Elmaci"'
Autor:
Pelin Ertan, Burcu Yazicioğlu, Hulya Nalcacioglu, Yeşim Özdemir Atikel, Neşe Bıyıklı, Alev Yilmaz, Duygu Övünç Hacıhamdioğlu, Sebahat Tulpar, Ayşe Ağbaş, Bahriye Atmis, Elif Çomak, Nimet Öner, Neslihan Cicek, Sibel Yel, Nuran Kucuk, Funda Bastug, Ibrahim Gökce, Ahmet Midhat Elmaci, Berfin Uysal, Binnaz Celik, Atilla Gemici, Neslihan Günay, Harika Alpay, Sema Akman, Ismail Dursun, Bağdagül Aksu, Fatma Sever, Serra Sürmeli Döven, Zeynep Nagehan Yürük Yildirim, Emine Özlem Çam Delebe, Ali Delibaş, Esra Karabağ Yilmaz
Tam Metin / Full Text Q4 PMID: 34174796 WOS:000724833600003 SCI-Expanded Nephrocalcinosis (NC) is defined as calcium deposition in the kidney parenchyma and tubules. This study aims to determine the etiology, risk factors, and follow-up results of pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53724520787fd933facabd21bfcd1cc5
https://hdl.handle.net/20.500.12712/33093
https://hdl.handle.net/20.500.12712/33093
Publikováno v:
Journal of Urological Surgery, Vol 10, Iss 2, Pp 112-118 (2023)
Objective:Information on cardiovascular problems related to childhood urinary stone disease is limited. The aim of this study was to assess the ventricular functions and subclinical cardiovascular risk in children with urolithiasis using echocardiogr
Externí odkaz:
https://doaj.org/article/4dc81ac1fb914742b735ae224ed73294
Publikováno v:
Dicle Medical Journal, Vol 40, Iss 3, Pp 369-373 (2013)
Volume: 40, Issue: 3 369-373
Dicle Tıp Dergisi
Volume: 40, Issue: 3 369-373
Dicle Tıp Dergisi
Amaç: Senkop özellikle çocukluk ve adolesan yaş grubunda daha sık olmakla birlikte her yaş grubunda görülebilen klinik bir problemdir. Bu çalışmada, vazovagal senkoplu hastalarda semptomların devamı ve medikal tedavi verilen hastalarda t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382cfe01d7ae90baf9f2a4216fd9f407
Publikováno v:
Pediatric Nephrology. 23:1009-1012
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), an autosomal recessive renal tubular disorder is characterized by the impaired tubular reabsorption of magnesium and calcium in the thick ascending limb of the loop of Henle. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2883e1a261ddfd6733542b277269bffb
https://doi.org/10.1007/s00467-008-0758-5
https://doi.org/10.1007/s00467-008-0758-5
Autor:
Oguz Soylemezoglu, Harun Peru, Necla Buyan, Sefika Elmas, Sevcan A. Bakkaloglu, Enver Hasanoglu, Davut Bozkaya, Fatih Kara, Ahmet Midhat Elmaci
Publikováno v:
Clinical Rheumatology. 27:1087-1092
We aimed to evaluate the patients who were diagnosed as Henoch Schonlein purpura (HSP) for disease characteristics and prognosis of those with joint, gastrointestinal (GI), and renal involvement. Two hundred and fifty-four children who were followed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f83a48f3289a75939ba8534c35a5a701
https://doi.org/10.1007/s10067-008-0868-2
https://doi.org/10.1007/s10067-008-0868-2
Autor:
Fatih Akın, Ahmet Midhat Elmaci
Publikováno v:
Volume: 41, Issue: 2 309-312
Dicle Tıp Dergisi
Dicle Tıp Dergisi
Objective: Congenital anomaly of kidney and urinary tract (CAKUT) includes functional and structural anomalies that can cause end-stage renal disease in children. Clinical and demographic characteristics of patients with CAKUT are evaluated in this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16f2ba13a87a51be9635612d7d66e358
https://dergipark.org.tr/tr/pub/dicletip/issue/4686/63829
https://dergipark.org.tr/tr/pub/dicletip/issue/4686/63829
Autor:
Ahmet Midhat Elmaci, Fatih Akin
Publikováno v:
Journal of Clinical and Experimental Investigations, Vol 5, Iss 1, Pp 128-130 (2014)
Hereditary xanthinuria is a novel autosomal recessive disorder of purine metabolism resulting from the deficiency of xanthine dehydrogenase. An 11-month-old boy admitted with the complaints of irritability for 6 months, darkening of the urine and spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d1889361e2b51740411135ac5c102c
https://doi.org/10.5799/ahinjs.01.2014.01.0377
https://doi.org/10.5799/ahinjs.01.2014.01.0377
Publikováno v:
Pediatric Nephrology. 22:1803-1805
Familial hypercholesterolemia (FH) is a common autosomal dominant inherited disorder characterized by increased levels of circulating plasma low-density lipoprotein cholesterol (LDL-C), tendon xanthomas, and premature atherosclerotic cardiovascular d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcf76b23a66bbe352f77ce5d10dee1bc
https://doi.org/10.1007/s00467-007-0534-y
https://doi.org/10.1007/s00467-007-0534-y
Objective: To report a case with the diagnosis of IgM nephropathy and familial Mediterranean fever (FMF). Clinical Presentation and Intervention: A 9-year-old boy was admitted to our hospital with recurrent abdominal pain since the age of 4 years. La
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcdb81c391a07ccffffc53b848f2c93b
http://hdl.handle.net/11655/13781
http://hdl.handle.net/11655/13781
Publikováno v:
Clinical rheumatology. 27(6)
The aim is to investigate whether pediatric familial Mediterranean fever (FMF) patients have an increased risk of premature atherosclerosis and to determine the possible strength of association between atherosclerosis and Mediterranean fever (MEFV) g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eaa16dbe6e51caa9255ab906fbcf52e
https://pubmed.ncbi.nlm.nih.gov/17926078
https://pubmed.ncbi.nlm.nih.gov/17926078