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The relation between increased carotid intima‐media thickness with fibrin monomers in obese children

International journal of clinical practice (Esher), 2021-07, Vol.75 (7), p.e14199-n/a

2021

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Risk factors for non-alcoholic fatty liver disease in obese children

Hormone research, 2009-01, Vol.72 (1), p.63-64

2009

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Goldenhar syndrome phenotypes and 22q11 deletion

American journal of medical genetics. Part A, 2011-02, Vol.155A (2), p.458-458

2011

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Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

Turkish journal of pediatrics, 2011-05, Vol.53 (3), p.274-280

2011

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Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies

American journal of medical genetics. Part A, 2006-03, Vol.140A (6), p.628-632

2006

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Growth hormone deficiency due to traumatic brain injury in a patient with X-linked congenital adrenal hypoplasia

Turkish journal of pediatrics, 2010-05, Vol.52 (3), p.312-316

2010

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Prevalence of obesity and associated risk factors among adolescents in Ankara, Turkey

Journal of clinical research in pediatric endocrinology, 2012-12, Vol.4 (4), p.204-207

2012

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EVALUATION OF GLUCOSE HOMEOSTASIS IN TRANSFUSION-DEPENDENT THALASSEMIC PATIENTS

Pediatric hematology and oncology, 2008-01, Vol.25 (7), p.630-637

2008

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Approach in an adolescent Proteus male patient with megafoot

Turkish journal of pediatrics, 2008-03, Vol.50 (2), p.200-203

2008

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Early prophylactic thyroidectomy for RET mutation-positive MEN 2B

Pediatrics international, 2009-08, Vol.51 (4), p.590-593

2009

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Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up

Journal of clinical research in pediatric endocrinology, 2008, Vol.1 (1), p.38-42

2008

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Evaluation of the Hypertension with Ambulatory Blood Pressure Monitoring in Obese Children

Life and Medical Sciences, 2022-05

2022

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A 19-year follow-up of a patient with type 3 ectrodactyly–ectodermal dysplasia–clefting syndrome who developed non-Hodgkin lymphoma

Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 2009-09, Vol.108 (3), p.e91-e95

2009

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Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia

Journal of Pediatric Endocrinology and Metabolism, 2012, Vol.25 (11-12), p.1205-1207

2012

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Letters to the Editor

The Cleft palate-craniofacial journal, 2010-07, Vol.47 (4), p.431-432

2010

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Letters to the Editor

The Cleft palate-craniofacial journal, 2010-07, Vol.47 (4), p.431-432

2010

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Letter to the Editor: Cleft palate and balanced de novo translocation t(6;7)(p25;q31)

The Cleft palate-craniofacial journal, 2010-02, p.100611121139056

2010

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Treatment of autonomous ovarian follicular cyst with long-term anastrozole therapy

Indian journal of pediatrics, 2009-09, Vol.76 (9), p.950-951

2009

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Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1–11.2;p13.3)

Developmental medicine and child neurology, 2007-03, Vol.49 (3), p.219-224

2007

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Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). Letter

The Cleft palate-craniofacial journal, 2010-07, Vol.47 (4), p.431-432

2010

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Early prophylactic thyroidectomy for RETmutation‐positive MEN 2B

Pediatrics international, 2009-08, Vol.51 (4), p.590-593

2009

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Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient

Journal of Pediatric Endocrinology and Metabolism, 2011-03, Vol.24 (1-2), p.109-112

2011

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LETTERS TO THE EDITOR

The Cleft palate-craniofacial journal, 2010-07, Vol.47 (4), p.430

2010

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Association of assisted reproductive technology with twinning and congenital anomalies

Indian journal of pediatrics, 2008-06, Vol.75 (6), p.638-640

2008

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Goldenhar syndrome phenotypes and 22q11 deletion

American journal of medical genetics. Part A, 2011, Vol.155A (2), p.458-458

2011

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The relation between increased carotid intima‐media thickness with fibrin monomers in obese children

Risk factors for non-alcoholic fatty liver disease in obese children

Goldenhar syndrome phenotypes and 22q11 deletion

Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies

Growth hormone deficiency due to traumatic brain injury in a patient with X-linked congenital adrenal hypoplasia

Prevalence of obesity and associated risk factors among adolescents in Ankara, Turkey

EVALUATION OF GLUCOSE HOMEOSTASIS IN TRANSFUSION-DEPENDENT THALASSEMIC PATIENTS

Approach in an adolescent Proteus male patient with megafoot

Early prophylactic thyroidectomy for RET mutation-positive MEN 2B

Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up

Evaluation of the Hypertension with Ambulatory Blood Pressure Monitoring in Obese Children

A 19-year follow-up of a patient with type 3 ectrodactyly–ectodermal dysplasia–clefting syndrome who developed non-Hodgkin lymphoma

Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia

Letters to the Editor

Letters to the Editor

Letter to the Editor: Cleft palate and balanced de novo translocation t(6;7)(p25;q31)

Treatment of autonomous ovarian follicular cyst with long-term anastrozole therapy

Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1–11.2;p13.3)

Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). Letter

Early prophylactic thyroidectomy for RETmutation‐positive MEN 2B

Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient

LETTERS TO THE EDITOR

Association of assisted reproductive technology with twinning and congenital anomalies

Goldenhar syndrome phenotypes and 22q11 deletion

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