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...

Is the Incidence of Congenital Hypothyroidism Really Increasing? A 20-Year Retrospective Population-Based Study in Québec

The journal of clinical endocrinology and metabolism, 2011-08, Vol.96 (8), p.2422-2429

2011

Volltextzugriff (PDF)

Redefining Congenital Hypothyroidism?

The journal of clinical endocrinology and metabolism, 2021-03, Vol.106 (3), p.e1463-e1465

2021

Volltextzugriff (PDF)

Practical Endocrinology and Diabetes in Children

Fourth edition., 2019

Volltextzugriff (PDF)

Premature Ovarian Failure in French Canadian Leigh Syndrome

The Journal of pediatrics, 2017-05, Vol.184, p.227-229.e1

2017

Volltextzugriff (PDF)

Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted?

European journal of endocrinology, 2017-11, Vol.177 (5), p.D1-D12

2017

Volltextzugriff (PDF)

Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome

The Journal of pediatrics, 2013-09, Vol.163 (3), p.800-805

2013

Volltextzugriff (PDF)

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism

American journal of human genetics, 2013-05, Vol.92 (5), p.725-743

2013

Volltextzugriff (PDF)

Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia: Benefits and costs of a successful public health program

M.S. Médecine sciences, 2021-05, Vol.37 (5), p.528

2021

Volltextzugriff (PDF)

Dépistage néonatal de l’hypothyroïdie congénitale et de l’hyperplasie congénitale des surrénales: Bénéfices et coûts d’un programme de santé publique à succès

M.S. Médecine sciences, 2021-05, Vol.37 (5), p.528-534

2021

Volltextzugriff (PDF)

Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia

International journal of neonatal screening, 2020-10, Vol.6 (4), p.82

2020

Volltextzugriff (PDF)

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (28), p.11524-11529

2011

Volltextzugriff (PDF)

Variation by ethnicity in the prevalence of congenital hypothyroidism due to thyroid dysgenesis

Thyroid (New York, N.Y.), 2011-01, Vol.21 (1), p.13-18

2011

Volltextzugriff (PDF)

Meeting Report: Measuring Endocrine-Sensitive Endpoints within the First Years of Life

Environmental health perspectives, 2008-07, Vol.116 (7), p.948-951

2008

Volltextzugriff (PDF)

Primary Adrenal Insufficiency in Children: Twenty Years Experience at the Sainte-Justine Hospital, Montreal

The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3243-3250

2005

Volltextzugriff (PDF)

Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis

American journal of human genetics, 2005-05, Vol.76 (5), p.729-749

2005

Volltextzugriff (PDF)

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary

Human mutation, 2005-05, Vol.25 (5), p.503-503

2005

Volltextzugriff (PDF)

Rising serum thyroxine levels and chorea in graves' disease

Pediatrics (Evanston), 2013-02, Vol.131 (2), p.e616-e619

2013

Volltextzugriff (PDF)

Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2009-11, Vol.94 (11), p.4380-4390

2009

Volltextzugriff (PDF)

Transcriptomic Signature of Human Embryonic Thyroid Reveals Transition From Differentiation to Functional Maturation

Frontiers in cell and developmental biology, 2021-06, Vol.9, p.669354-669354

2021

Volltextzugriff (PDF)

Interpreting Minor Variations in Thyroid Function or Echostructure

The Pediatric clinics of North America, 2015-08, Vol.62 (4), p.929-942

2015

Volltextzugriff (PDF)

Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

BMC pediatrics, 2011-05, Vol.11 (1), p.49-49, Article 49

2011

Volltextzugriff (PDF)

Apparent Manifesting Heterozygosity in P450 Oxidoreductase Deficiency and Its Effect on Coexisting 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2007-06, Vol.92 (6), p.2318-2322

2007

Volltextzugriff (PDF)

Are Guidelines for Glucocorticoid Coverage in Adrenal Insufficiency Currently Followed?

The Journal of pediatrics, 2011-03, Vol.158 (3), p.492-498.e1

2011

Volltextzugriff (PDF)

Leydig Cell Tumors in Children: Contrasting Clinical, Hormonal, Anatomical, and Molecular Characteristics in Boys and Girls

The Journal of pediatrics, 2012-12, Vol.161 (6), p.1147-1152

2012

Volltextzugriff (PDF)

A Search for Variables Predicting Cortisol Response to Low-Dose Corticotropin Stimulation Following Supraphysiological Doses of Glucocorticoids

The Journal of pediatrics, 2013-08, Vol.163 (2), p.484-488.e1

2013

Volltextzugriff (PDF)

1 – 25 von 247

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(204)
Mit Volltextzugriff
(197)

Publikationsform

Artikel
(211)
Buchkapitel
(31)
Berichte
(3)
Bücher
(2)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(143)
Life Sciences & Biomedicine
(138)
Humans
(128)
Female
(88)
Male
(77)
Endocrinology & Metabolism
(71)
Biological And Medical Sciences
(64)
Medical Sciences
(56)
Pediatrics
(53)
Child
(47)
Infant, Newborn
(45)
Adolescent
(37)
Endocrinopathies
(32)
Child, Preschool
(28)
Congenital Hypothyroidism
(28)
Infant
(28)
Mutation
(26)
Fundamental And Applied Biological Sciences. Psychology
(23)
Non Tumoral Diseases. Target Tissue Resistance. Benign Neoplasms
(23)
Neonatal Screening
(18)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Is the Incidence of Congenital Hypothyroidism Really Increasing? A 20-Year Retrospective Population-Based Study in Québec

Redefining Congenital Hypothyroidism?

Practical Endocrinology and Diabetes in Children

Premature Ovarian Failure in French Canadian Leigh Syndrome

Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted?

Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism

Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia: Benefits and costs of a successful public health program

Dépistage néonatal de l’hypothyroïdie congénitale et de l’hyperplasie congénitale des surrénales: Bénéfices et coûts d’un programme de santé publique à succès

Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

Variation by ethnicity in the prevalence of congenital hypothyroidism due to thyroid dysgenesis

Meeting Report: Measuring Endocrine-Sensitive Endpoints within the First Years of Life

Primary Adrenal Insufficiency in Children: Twenty Years Experience at the Sainte-Justine Hospital, Montreal

Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary

Rising serum thyroxine levels and chorea in graves' disease

Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Transcriptomic Signature of Human Embryonic Thyroid Reveals Transition From Differentiation to Functional Maturation

Interpreting Minor Variations in Thyroid Function or Echostructure

Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

Apparent Manifesting Heterozygosity in P450 Oxidoreductase Deficiency and Its Effect on Coexisting 21-Hydroxylase Deficiency

Are Guidelines for Glucocorticoid Coverage in Adrenal Insufficiency Currently Followed?

Leydig Cell Tumors in Children: Contrasting Clinical, Hormonal, Anatomical, and Molecular Characteristics in Boys and Girls

A Search for Variables Predicting Cortisol Response to Low-Dose Corticotropin Stimulation Following Supraphysiological Doses of Glucocorticoids

Suchergebnisse filtern