UB Paderborn / Katalog / Suche / in CDI

Current concepts in disorders of sexual development

Journal of clinical research in pediatric endocrinology, 2011, Vol.3 (3), p.105-114

Öçal, Gönül

2011

Volltextzugriff (PDF)

Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study

Journal of clinical research in pediatric endocrinology, 2013-01, Vol.5 (1), p.20-26

2013

Volltextzugriff (PDF)

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

Journal of Pediatric Endocrinology and Metabolism, 2011-03, Vol.24 (1-2), p.21-24

2011

Volltextzugriff (PDF)

Adherence to growth hormone therapy: results of a multicenter study

Endocrine practice, 2014-01, Vol.20 (1), p.46-51

2014

Volltextzugriff (PDF)

Depression, levels of anxiety and self-concept in girls with Turner's syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2005-11, Vol.18 (11), p.1111

2005

Volltextzugriff (PDF)

Primary amenorrhea in four adolescents revealed 5α-reductase deficiency confirmed by molecular analysis

Fertility and sterility, 2011-02, Vol.95 (2), p.804.e1-804.e5

2011

Volltextzugriff (PDF)

The incidence and evolution of thyroid dysfunction during interferon-alpha therapy in children with chronic hepatitis B infection

Journal of pediatric endocrinology & metabolism : JPEM, 2007-02, Vol.20 (2), p.237

2007

Volltextzugriff (PDF)

Hypophosphatasia associated with Pseudotumor cerebri and respiratory insufficiency

Indian journal of pediatrics, 2008-02, Vol.75 (2), p.186-188

2008

Volltextzugriff (PDF)

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

American journal of human genetics, 2013-01, Vol.92 (1), p.131-136

2013

Volltextzugriff (PDF)

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?

European journal of pediatrics, 2012-10, Vol.171 (10), p.1497-1502

2012

Volltextzugriff (PDF)

Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4260-4266

2005

Volltextzugriff (PDF)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.211-217

2016

Volltextzugriff (PDF)

The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

Journal of pediatric endocrinology & metabolism : JPEM, 2014-09, Vol.27 (9-10), p.901

2014

Volltextzugriff (PDF)

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

Endocrine, 2015-06, Vol.49 (2), p.479-491

2015

Volltextzugriff (PDF)

Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents

Ultrasound in medicine & biology, 2014-05, Vol.40 (5), p.871-876

2014

Volltextzugriff (PDF)

A Novel Heterozygous Mutation in Steroidogenic Factor-1 in Pubertal Virilization of a 46,XY Female Adolescent

Journal of pediatric & adolescent gynecology, 2014-04, Vol.27 (2), p.98-101

2014

Volltextzugriff (PDF)

Relationships between osteocalcin, glucose metabolism, and adiponectin in obese children: Is there crosstalk between bone tissue and glucose metabolism?

Journal of clinical research in pediatric endocrinology, 2012-12, Vol.4 (4), p.182-188

2012

Volltextzugriff (PDF)

Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Journal of pediatric & adolescent gynecology, 2015-02, Vol.28 (1), p.6-11

2015

Volltextzugriff (PDF)

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

Journal of Pediatric Endocrinology and Metabolism, 2011-12, Vol.24 (11-12), p.1019-1023

2011

Volltextzugriff (PDF)

Pathophysiology of critical illness hyperglycemia in children

Journal of Pediatric Endocrinology and Metabolism, 2013, Vol.26 (7-8), p.715-720

2013

Volltextzugriff (PDF)

Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model

Turkish journal of pediatrics, 2007-04, Vol.49 (2), p.165-170

2007

Volltextzugriff (PDF)

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

Clinical and applied thrombosis/hemostasis, 2011-11, Vol.17 (6), p.585-589

2011

Volltextzugriff (PDF)

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

Journal of Pediatric Endocrinology and Metabolism, 2011-12, Vol.24 (11-12), p.1077-1080

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Vitamin D deficiency in Turkish mothers and their neonates and in women of reproductive age

Journal of clinical research in pediatric endocrinology, 2009-12, Vol.1 (6), p.266-269

2009

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Current concepts in disorders of sexual development

Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

Adherence to growth hormone therapy: results of a multicenter study

Depression, levels of anxiety and self-concept in girls with Turner's syndrome

Primary amenorrhea in four adolescents revealed 5α-reductase deficiency confirmed by molecular analysis

The incidence and evolution of thyroid dysfunction during interferon-alpha therapy in children with chronic hepatitis B infection

Hypophosphatasia associated with Pseudotumor cerebri and respiratory insufficiency

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?

Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents

A Novel Heterozygous Mutation in Steroidogenic Factor-1 in Pubertal Virilization of a 46,XY Female Adolescent

Relationships between osteocalcin, glucose metabolism, and adiponectin in obese children: Is there crosstalk between bone tissue and glucose metabolism?

Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

Pathophysiology of critical illness hyperglycemia in children

Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

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

Vitamin D deficiency in Turkish mothers and their neonates and in women of reproductive age

Suchergebnisse filtern