Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Utku Erdem Soyaltin"'
Autor:
Utku Erdem Soyaltin, Ilgin Yildirim Simsir, Baris Akinci, Canan Altay, Suleyman Cem Adiyaman, Kristen Lee, Huseyin Onay, Elif Arioglu Oral
Publikováno v:
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-6 (2020)
Abstract Background Classical heterozygous pathogenic variants of the lamin A/C (LMNA) gene cause autosomal dominant familial partial lipodystrophy type 2 (FPLD2). However, recent reports indicate phenotypic heterogeneity among carriers of LMNA patho
Externí odkaz:
https://doaj.org/article/c3c96ebba42c468a8310e376132b3b67
Autor:
Ilgin Yildirim Simsir, Beyhan Tuysuz, Mehmet Nuri Ozbek, Seher Tanrikulu, Merve Celik Guler, Asuman Nur Karhan, Yasemin Denkboy Ongen, Nilay Gunes, Utku Erdem Soyaltin, Canan Altay, Banu Nur, Servan Ozalkak, Ozlem Akgun Dogan, Fatma Dursun, Zafer Pekkolay, Mehmet Ali Eren, Yusuf Usta, Secil Ozisik, Basak Ozgen Saydam, Suleyman Cem Adiyaman, Mehmet Cagri Unal, Gokcen Gungor Semiz, Ihsan Turan, Erdal Eren, Hulya Kayserili, Isabelle Jeru, Corinne Vigouroux, Tahir Atik, Huseyin Onay, Samim Ozen, Elif Arioglu Oral, Baris Akinci
Aim: To describe the Turkish generalized lipodystrophy (GL) cohort with the frequency of each complication and the death rate during the period of the follow-up. Methods: This study reports on 72 patients with GL (47 families) registered at different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b8d0fd4a5c946862cce5364ffbbd6bd
https://avesis.deu.edu.tr/publication/details/497e612a-1225-4cce-8c09-189e93672690/oai
https://avesis.deu.edu.tr/publication/details/497e612a-1225-4cce-8c09-189e93672690/oai
Autor:
null Ilgin Yildirim Simsir, null Beyhan Tuysuz, null Mehmet Nuri Ozbek, null Seher Tanrikulu, null Merve Celik Guler, null Asuman Nur Karhan, null Yasemin Denkboy Ongen, null Nilay Gunes, null Utku Erdem Soyaltin, null Canan Altay, null Banu Nur, null Servan Ozalkak, null Ozlem Akgun Dogan, null Fatma Dursun, null Zafer Pekkolay, null Mehmet Ali Eren, null Yusuf Usta, null Secil Ozisik, null Basak Ozgen Saydam, null Suleyman Cem Adiyaman, null Mehmet Cagri Unal, null Gokcen Gungor Semiz, null Ihsan Turan, null Erdal Eren, null Hulya Kayserili, null Isabelle Jeru, null Corinne Vigouroux, null Tahir Atik, null Huseyin Onay, null Samim Ozen, null Elif A. Oral, null Baris Akinci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01db91016594b1eb67c4f96799aa4507
https://doi.org/10.1111/dom.15061/v2/response1
https://doi.org/10.1111/dom.15061/v2/response1
Publikováno v:
Hormones (Athens, Greece).
Acromegaly is a disease with various comorbidities and hypogonadism is a common comorbidity in patients with acromegaly. Herein, we aim to present our experience with clomiphene citrate in a patient with acromegaly accompanied by hypogonadism, who de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2e59c22d2093841cec21ba17611f8b8
https://pubmed.ncbi.nlm.nih.gov/36344736
https://pubmed.ncbi.nlm.nih.gov/36344736
Autor:
Utku Erdem Soyaltin, Deniz Yuce Yildirim, Mustafa Yildirim, Mehmet Can Ugur, Ferhat Ekinci, Cengiz Ceylan, Harun Akar
Publikováno v:
Case Reports in Hematology, Vol 2016 (2016)
We report a 63-year-old man with a history of chronic lymphocytic leukemia (CLL) who presented with asymmetrical Raynaud’s phenomenon of sudden onset which progressed to acral gangrene rapidly in a week. These symptoms began approximately one week
Externí odkaz:
https://doaj.org/article/c5986822706940ecb0bd7a71d59c56d3
Publikováno v:
Endocrine. 64:118-121
Persistent elevation of thyroid-stimulating hormone (TSH) is common in endocrinology practice in patients undergoing replacement or suppression therapy with levothyroxine sodium (LT4). After examining the causes of this condition, LT4 absorption test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1046b888f49066f327c89f2e8f483ccf
https://doi.org/10.1007/s12020-019-01889-x
https://doi.org/10.1007/s12020-019-01889-x
Aim: Glucose is an osmotic agent in the peritoneal dialysis fluid (PDF) to absorb water, sodium and other toxins. Glucose absorption from PDF to blood impairs peritoneal dialysis (PD) efficiency and cause glycemic burden. This extra glycemic load lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1274961c8c529719127d9863927806ef
https://hdl.handle.net/11454/80690
https://hdl.handle.net/11454/80690
Publikováno v:
Endocrine
[No Abstract Available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a3e8772b8b7d8d7dbd8345ffdc04c38
https://hdl.handle.net/11454/76253
https://hdl.handle.net/11454/76253
Autor:
Suleyman Cem Adiyaman, Hüseyin Onay, Baris Akinci, Elif A. Oral, Ilgin Yildirim Simsir, Utku Erdem Soyaltin, Kristen N. Lee, Canan Altay
Publikováno v:
Clinical Diabetes and Endocrinology
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-6 (2020)
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-6 (2020)
Background Classical heterozygous pathogenic variants of the lamin A/C (LMNA) gene cause autosomal dominant familial partial lipodystrophy type 2 (FPLD2). However, recent reports indicate phenotypic heterogeneity among carriers of LMNA pathogenic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f5d3422c43ce79b30cb60fcd0d75dc
https://doi.org/10.1186/s40842-020-00100-9
https://doi.org/10.1186/s40842-020-00100-9
Autor:
Suleyman Cem Adiyaman, Ilgin Yildirim Simsir, Canan Altay, Elif A. Oral, Utku Erdem Soyaltin, Baris Akinci
Publikováno v:
Journal of the Endocrine Society
Background Classical heterozygous pathogenic variants of the lamin A/C (LMNA) gene cause familial partial lipodystrophy type 2 (FPLD2). However, recent reports indicate phenotypic heterogeneity among carriers of LMNA pathogenic variants, and a few pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd2be59d67c47db49f81480b275da1cb
https://doi.org/10.1210/jendso/bvaa046.1122
https://doi.org/10.1210/jendso/bvaa046.1122