Zobrazeno 1 - 10
of 196
pro vyhledávání: '"K Tinaztepe"'
Autor:
Franz Petry, Aysin Bakkaloglu, Michael Loos, Ersoy F, A. I. Berkel, K. Tinaztepe, Ozden Sanal
Publikováno v:
European Journal of Pediatrics. 156:113-115
A 7-year-old male with recurrent erythematous and desquamated skin lesions and respiratory infections was diagnosed as selective complete C1q deficiency following detailed studies of the complement system. His asymptomatic sister also had selective c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8ad4357113d4df8343b519c645734c
https://doi.org/10.1007/s004310050567
https://doi.org/10.1007/s004310050567
Publikováno v:
The Turkish journal of pediatrics. 43(2)
Apoptosis, a programmed form of cell death, is an important mechanism that maintains cellular homeostasis. The cellular content of tissues is regulated by a balance between cell proliferation and cell loss. Apoptosis is important not only in physiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2520bad7132edfad342ce28187e29d12
https://pubmed.ncbi.nlm.nih.gov/11432492
https://pubmed.ncbi.nlm.nih.gov/11432492
Publikováno v:
The Turkish journal of pediatrics. 42(2)
The purpose of this study was to investigate children followed as having both Hodgkin's disease (HD) and nephropathy and discuss the factors which might play roles in the pathogenesis of this association by reviewing the pertinent literature. Our exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f73f9da2c8b7671b85b006506152a5f
https://pubmed.ncbi.nlm.nih.gov/10936975
https://pubmed.ncbi.nlm.nih.gov/10936975
Publikováno v:
The Turkish journal of pediatrics. 42(1)
Cyclic neutropenia is a rare disease characterized by regular cyclic fluctuations in the numbers of neutrophils. Patients with the disease suffer from recurrent infections at regular intervals of nearly three weeks. Recently, recombinant human granul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a0e2bfe2dd1c2410376fc017b17cbb5
https://pubmed.ncbi.nlm.nih.gov/11432504
https://pubmed.ncbi.nlm.nih.gov/11432504
Publikováno v:
The Turkish journal of pediatrics. 40(2)
Infantile oxalosis is a rare, autosomal recessive disorder. We present three unrelated cases of infantile oxalosis and their families, emphasizing its place as a cause of acute renal failure in infancy, and showing the clinical heterogeneity of the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a83c64a3b50679511c010f838aa61b9f
https://pubmed.ncbi.nlm.nih.gov/9677729
https://pubmed.ncbi.nlm.nih.gov/9677729
Publikováno v:
The Turkish journal of pediatrics. 39(2)
Three cases with hepatitis B virus (HBV)-related, biopsy-diagnosed glomerulopathies, one of which was membranous glomerulonephritis and the others membranoproliferative glomerulonephritis, are reported, emphasizing the clinical course. Two patients h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e53af6ccf897c5168ef9fac8d77d871
https://pubmed.ncbi.nlm.nih.gov/9223922
https://pubmed.ncbi.nlm.nih.gov/9223922
Autor:
K, Tinaztepe
Publikováno v:
The Turkish journal of pediatrics. 38(2)
In this article, the publication potential in pediatrics in Turkey was investigated. In this context, native pediatric journals, publication activities of medical faculties as the main source of scientific publication and certain data obtained from s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::43d6002ee37178d86c9cc51b73553585
https://pubmed.ncbi.nlm.nih.gov/8701486
https://pubmed.ncbi.nlm.nih.gov/8701486
Publikováno v:
The Turkish journal of pediatrics. 38(1)
We present a 12-year-old boy who developed subacute thyroiditis during the course of rapidly progressive glomerulonephritis due to Henoch-Schonlein purpura (HSP) proven by clinical findings and percutaneous renal needle biopsy. The thyroid gland of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a13283e1415bc9bcd98f64bdfd2335d
https://pubmed.ncbi.nlm.nih.gov/8819634
https://pubmed.ncbi.nlm.nih.gov/8819634
Autor:
K, Tinaztepe
Publikováno v:
The Turkish journal of pediatrics. 37(4)
Amyloidosis is a heterogeneous group of diseases characterized by extracellular accumulation of an eosinophilic, hyalin and proteinaceous material containing mucopolysaccharide substance in various tissues and organs. Knowledge about the chemical str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d0165bf0f2da0ab3aef26c2df20838a
https://pubmed.ncbi.nlm.nih.gov/8560604
https://pubmed.ncbi.nlm.nih.gov/8560604
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 10(1)
Four and two male sibs of two separate families who had biopsy-proven membranoproliferative glomerulonephritis (MPGN) are presented. In the first family four sibs of the first-degree consanguineous marriage showed the clinical picture of nephrotic sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac2fe0cd1d147b8f5e02e07cc4e3c114
https://pubmed.ncbi.nlm.nih.gov/7724023
https://pubmed.ncbi.nlm.nih.gov/7724023