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Hypogonadotropic Hypogonadism due to Novel FGFR1 MutationsIdiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.Prevalence of Neisseria meningitidis carriage: a small-scale survey in Istanbul, Turkey.Sleep disordered breathing and sleep quality in children with bronchiolitis obliterans.CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance.Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide.The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transientAn infant with hyponatremia, hyperkalemia, and metabolic acidosis associated with urinary tract infection: QuestionsAn infant with hyponatremia, hyperkalemia, and metabolic acidosis associated with urinary tract infection: AnswersEfficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for CraniopharyngiomaDetermination of cerebral edema with serial measurement of optic nerve sheath diameter during treatment in children with diabetic ketoacidosis: a longitudinal studyUnusual and early onset IPEX syndrome: a case reportPrevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism
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P50
description
researcher ORCID ID = 0000-0002-5654-247X
@en
wetenschapper
@nl
name
Ihsan Turan
@ast
Ihsan Turan
@en
Ihsan Turan
@es
Ihsan Turan
@nl
type
label
Ihsan Turan
@ast
Ihsan Turan
@en
Ihsan Turan
@es
Ihsan Turan
@nl
prefLabel
Ihsan Turan
@ast
Ihsan Turan
@en
Ihsan Turan
@es
Ihsan Turan
@nl
P1153
56982700100
P31
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0000-0002-5654-247X