Yusuf K. Haspolat

Dicle, Turkey

Last Updated: 09/26/2026

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Found 17 publications

Evaluation of Clinical and Laboratory Findings in the Differential Diagnosis of Central Precocious Puberty and Premature Thelarche.

Evaluation of Clinical and Laboratory Findings in the Differential Diagnosis of Central Precocious Puberty and Premature Thelarche.

Journal: Indian journal of endocrinology and metabolism

Published: June 20, 2022

Is cranial imaging necessary in girls between 6-8 years diagnosed with central precocious puberty?

Is cranial imaging necessary in girls between 6-8 years diagnosed with central precocious puberty?

Journal: Minerva endocrinology

Published: September 21, 2021

A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.

A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.

Journal: Endocrine

Published: July 01, 2021

The association between electrocardiographic data and obesity in children and adolescents.

The association between electrocardiographic data and obesity in children and adolescents.

Journal: Minerva pediatrics

Published: April 16, 2021

Evaluation of anterior segment parameters with Pentacam in children with poorly-controlled type 1 Diabetes Mellitus without diabetic retinopathy.

Evaluation of anterior segment parameters with Pentacam in children with poorly-controlled type 1 Diabetes Mellitus without diabetic retinopathy.

Journal: Photodiagnosis and photodynamic therapy

Published: December 03, 2020

A DIFFERENT PERSPECTIVE OF ELEVATED LACTATE IN PEDIATRIC PATIENTS WITH DIABETIC KETOACIDOSIS.

A DIFFERENT PERSPECTIVE OF ELEVATED LACTATE IN PEDIATRIC PATIENTS WITH DIABETIC KETOACIDOSIS.

Journal: Acta endocrinologica (Bucharest, Romania : 2005)

Published: July 21, 2020

A novel variant in LCHGR gene in 3 siblings with type 1 Leydig cell hypoplasia.

A novel variant in LCHGR gene in 3 siblings with type 1 Leydig cell hypoplasia.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: July 14, 2020

Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families.

Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families.

Journal: Journal of endocrinological investigation

Published: July 13, 2020

A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene.

A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: December 31, 2019

Left and right ventricular functions may be impaired in children diagnosed with subclinical hypothyroidism.

Left and right ventricular functions may be impaired in children diagnosed with subclinical hypothyroidism.

Journal: Scientific reports

Published: August 23, 2019

Subclinical hypothyroidism and long QT.

Subclinical hypothyroidism and long QT.

Journal: Pacing and clinical electrophysiology : PACE

Published: July 13, 2018

A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct Syndrome

A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct Syndrome

Journal: Journal of clinical research in pediatric endocrinology

Published: April 25, 2018

Showing 1-12 of 17

Last Updated: 09/26/2026