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Showing page 1 of results 1 - 10 of about 14 matches for "seber-selcuk"

100% match
2 hit(s)
PDF
325kb

10.3252/pso.eu.55ESPE.2016

http://abstracts.eurospe.org//hrp/0086/eposters/hrp0086p1-p109_eposter.pdf
Published:

100% match
2 hit(s)
PDF
325kb

10.3252/pso.eu.55ESPE.2016

http://abstracts.eurospe.org/hrp/0086/eposters/hrp0086p1-p109_eposter.pdf
Published:

85% match
6 hit(s)
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Comparison of various insulin sensivity indices in idiopathic hirsutism
Sema Ucak; Okcan Basat; Selcuk Seber; Emine Satir; Cigdem Y Ersoy
http://www.endocrine-abstracts.org/ea/0011/ea0011p700.htm
Published: 2006-12-04

85% match
6 hit(s)
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Effects of metformin therapy in lean subjects with pcos on insulin resistance indices
Yuksel Altuntas; Okcan Basat; Sema Ucak; Selcuk Seber; Nezake Eren; Cigdem Y Ersoy; Kubra Arslan
http://www.endocrine-abstracts.org/ea/0011/ea0011p699.htm
Published: 2006-12-04

85% match
6 hit(s)
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Prolonged hungry bone syndrome in a patient with wolfram syndrome: a case report
Okcan Basat; Sema Ucak; Ahsen Bas Oncul; Selcuk Seber; Nezake Eren; Yuksel Altuntas
http://www.endocrine-abstracts.org/ea/0011/ea0011p144.htm
Published: 2006-12-04

50% match
2 hit(s)
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Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta
Saygin Abali; Ahmet Arman; Zeynep Atay; Serpil Bas; Sevda Cam; Zeliha Gormez; Huseyin Demirci; Yasemin Alanay; Nurten Akarsu; Ab
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p109.htm
Published: 2016-08-19

42% match
2 hit(s)
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Unique occurrence of long bone fragility with cranial hyperostosis: Searching for the genetic culprit
Adalbert Raimann; Uwe Wintergerst; Paul Roschger; Rainer Stelzl; Rainer Biedermann; Michael Rasse; Nadja Fratzl-Zelman; Franco L
http://www.bone-abstracts.org/ba/0004/ba0004p108.htm
Published: 2015-06-09

28% match
2 hit(s)
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Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems | ESPE2019
Laura Guazzarotti; Sara Azzolini; Sheila Ulivi; Antonella Fabretto; Francesca Riello; Carmela Ardisia
http://abstracts.eurospe.org/hrp/0092/hrp0092LB-22
Published: 2019-08-22

28% match
2 hit(s)
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Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems | ESPE2019
Laura Guazzarotti; Sara Azzolini; Sheila Ulivi; Antonella Fabretto; Francesca Riello; Carmela Ardisia
http://abstracts.eurospe.org/hrp/0092/hrp0092lb-22.html
Published: 2019-08-22

28% match
2 hit(s)
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33kb

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