UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Unusual presentation of a recurrent squamous cell lung cancer

QJM : An International Journal of Medicine, 2015-03, Vol.108 (3), p.231-232

2015

Volltextzugriff (PDF)

The course of spinal tuberculosis (Pott disease): results of the multinational, multicentre Backbone-2 study

Clinical microbiology and infection, 2015-11, Vol.21 (11), p.1008.e9-1008.e18

2015

Volltextzugriff (PDF)

Persistently Raised Thyroid Stimulating Hormone in Adequately Treated Congenital Hypothyroidism on Long-term Follow-up

Journal of Pediatric Endocrinology and Metabolism, 2008, Vol.21 (3), p.251-256

2008

Volltextzugriff (PDF)

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A376-A377

2012

Volltextzugriff (PDF)

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Experimental and clinical endocrinology & diabetes, 2009-06, Vol.117 (6), p.301-304

2009

Volltextzugriff (PDF)

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

Journal of Pediatric Endocrinology and Metabolism, 2010-11, Vol.23 (11), p.1123-1132

2010

Volltextzugriff (PDF)

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Experimental and clinical endocrinology & diabetes, 2009-07, Vol.117 (7), p.312-315

2009

Volltextzugriff (PDF)

Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty

Journal of Pediatric Endocrinology and Metabolism, 2003-03, Vol.16 (3), p.407

2003

Volltextzugriff (PDF)

Management of central diabetes insipidus with oral desmopressin in a premature neonate

Journal of Pediatric Endocrinology and Metabolism, 2004-02, Vol.17 (2), p.227

2004

Volltextzugriff (PDF)

Primary Penile Squamous Cell Cancer-Related Malignant Priapism in a Cystectomized Patient: A Case Report

Curēus (Palo Alto, CA), 2022-11

2022

Volltextzugriff (PDF)

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Journal of Pediatric Endocrinology and Metabolism, 2006-05, Vol.19 (5), p.741

2006

Volltextzugriff (PDF)

Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

Experimental and clinical endocrinology & diabetes, 2009-02, Vol.117 (2), p.57-59

2009

Volltextzugriff (PDF)

Congenital early onset isolated adrenocorticotropin deficiency associated with a TPIT gene mutation

Journal of Pediatric Endocrinology and Metabolism, 2004-07, Vol.17 (7), p.1017

2004

Volltextzugriff (PDF)

No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey

Journal of Pediatric Endocrinology and Metabolism, 2002-07, Vol.15 (7), p.1033

2002

Volltextzugriff (PDF)

Osteopetrosis, renal tubular acidosis without urinary concentration abnormality, cerebral calcification and severe mental retardation in three Turkish brothers

Journal of Pediatric Endocrinology and Metabolism, 2001-11, Vol.14 (9), p.1671

2001

Volltextzugriff (PDF)

Severe hypercalcemia of an infant due to vitamin D toxicity associated with hypercholesterolemia

Journal of Pediatric Endocrinology and Metabolism, 2001-07, Vol.14 (7), p.915

2001

Volltextzugriff (PDF)

Factors contributing to sex assignment and reassignment decisions in Turkish children with 46,XY disorders of sex development

Journal of Pediatric Endocrinology and Metabolism, 2007-09, Vol.20 (9), p.1001

2007

Volltextzugriff (PDF)

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Journal of Pediatric Endocrinology and Metabolism, 2005-01, Vol.18 (10), p.949

2005

Volltextzugriff (PDF)

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Journal of Pediatric Endocrinology and Metabolism, 2008-08, Vol.21 (8), p.781-788

2008

Volltextzugriff (PDF)

Efficacy of levamisole on experimental endometriosis

International journal of gynecology and obstetrics, 2007-10, Vol.99 (1), p.38-42

2007

Volltextzugriff (PDF)

Association of partial gonadal dysgenesis, nephropathy and WT1 gene mutation without Wilms' tumor: incomplete Denys-Drash syndrome

Journal of Pediatric Endocrinology and Metabolism, 2001-05, Vol.14 (5), p.561

2001

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)

A new deletion of the 5α-reductase type 2 gene in a Turkish family with 5α-reductase deficiency

Clinical endocrinology (Oxford), 1995-08, Vol.43 (2), p.183-188

1995

Volltextzugriff (PDF)

The Incidence and Evolution of Thyroid Dysfunction During Interferon-α Therapy in Children with Chronic Hepatitis Β Infection

Journal of Pediatric Endocrinology and Metabolism, 2007-01, Vol.20 (2)

2007

Volltextzugriff (PDF)

The Influence of Interferon-α and Combination Interferon-α and Lamivudine Therapy on Height and Weight in Children with Chronic Hepatitis Β Infection

Journal of Pediatric Endocrinology and Metabolism, 2007-01, Vol.20 (5)

2007

Volltextzugriff (PDF)

1 – 25 von 197

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(177)
Mit Volltextzugriff
(135)

Publikationsform

Sprache

Englisch
(194)
Türkisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Unusual presentation of a recurrent squamous cell lung cancer

The course of spinal tuberculosis (Pott disease): results of the multinational, multicentre Backbone-2 study

Persistently Raised Thyroid Stimulating Hormone in Adequately Treated Congenital Hypothyroidism on Long-term Follow-up

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty

Management of central diabetes insipidus with oral desmopressin in a premature neonate

Primary Penile Squamous Cell Cancer-Related Malignant Priapism in a Cystectomized Patient: A Case Report

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

Congenital early onset isolated adrenocorticotropin deficiency associated with a TPIT gene mutation

No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey

Osteopetrosis, renal tubular acidosis without urinary concentration abnormality, cerebral calcification and severe mental retardation in three Turkish brothers

Severe hypercalcemia of an infant due to vitamin D toxicity associated with hypercholesterolemia

Factors contributing to sex assignment and reassignment decisions in Turkish children with 46,XY disorders of sex development

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Efficacy of levamisole on experimental endometriosis

Association of partial gonadal dysgenesis, nephropathy and WT1 gene mutation without Wilms' tumor: incomplete Denys-Drash syndrome

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

A new deletion of the 5α-reductase type 2 gene in a Turkish family with 5α-reductase deficiency

The Incidence and Evolution of Thyroid Dysfunction During Interferon-α Therapy in Children with Chronic Hepatitis Β Infection

The Influence of Interferon-α and Combination Interferon-α and Lamivudine Therapy on Height and Weight in Children with Chronic Hepatitis Β Infection

Suchergebnisse filtern