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Analysis of the Wilms' Tumor Suppressor Gene (WT1) in Patients 46,XY Disorders of Sex Development

The journal of clinical endocrinology and metabolism, 2011-07, Vol.96 (7), p.E1131-E1136

2011

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Thyroid dysfunction in pregnancy

Deutsche medizinische Wochenschrift (1946), 2014-10, Vol.139 (42), p.2148

2014

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Schilddrüsenerkrankungen im Kindes- und Jugendalter

Monatsschrift Kinderheilkunde, 2015-06, Vol.163 (6), p.601-615

Krude, H.

2015

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Diagnostik seltener Erkrankungen in der Pädiatrie

Monatsschrift Kinderheilkunde, 2022, Vol.170 (1), p.13-20

2022

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Is there a further acceleration in the age at onset of menarche? A cross-sectional study in 1840 school children focusing on age and bodyweight at the onset of menarche

European journal of endocrinology, 2009-01, Vol.160 (1), p.107-113

2009

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Metastabile Epiallele – beeinflussen epigenetische Varianten das individuelle Adipositasrisiko?

Adipositas - Ursachen, Folgeerkrankungen, Therapie, 2018-12, Vol.12 (4), p.183-188

2018

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Development of a pediatric differentiated thyroid carcinoma registry within the EuRRECa project: rationale and protocol

Endocrine Connections, 2023-03, Vol.12 (3), p.1-9

2023

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Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis

The journal of clinical endocrinology and metabolism, 2010-07, Vol.95 (7), p.3446-3452

2010

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No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2010-05, Vol.95 (5), p.2443-2450

2010

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Impaired glucose tolerance and type 2 diabetes mellitus: a new field for pediatrics in Europe

International Journal of Obesity, 2005-09, Vol.29 (S2), p.S136-S142

2005

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Two puzzling cases of thyroid dysgenesis

Hormone research, 2009-01, Vol.71 Suppl 1 (Suppl. 1), p.93-97

2009

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Treating patients not numbers: the benefit and burden of lowering TSH newborn screening cut-offs

Archives of disease in childhood, 2011-02, Vol.96 (2), p.121-122

2011

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Ethnicity and comorbidities in an overweight and obese multiethnic childhood cohort in Berlin

Acta Paediatrica, 2011-04, Vol.100 (4), p.578-584

2011

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How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4562-4567

2000

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Schilddrüsenhormon und Störungen des Zentralnervensystems

Monatsschrift Kinderheilkunde, 2008-10, Vol.156 (10), p.961-971

Krude, H.

2008

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Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review

Neuropsychiatric disease and treatment, 2023-10, Vol.19, p.2195-2216

2023

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Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

The Lancet (British edition), 2004-10, Vol.364 (9443), p.1435-1437

2004

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Schilddrüsenfunktionsstörungen in der Schwangerschaft

Deutsche medizinische Wochenschrift, 2014-10, Vol.139 (42), p.2148-2152

2014

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Partielle Lipodystrophie mit Verdacht auf Autoimmunerkrankung

Arthritis + Rheuma, 2019-10, Vol.39 (5), p.341-343

2019

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Consensus statement : Childhood obesity

The journal of clinical endocrinology and metabolism, 2005-03, Vol.90 (3), p.1871-1887

2005

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Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

Nature genetics, 1998-06, Vol.19 (2), p.155-157

1998

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Obesity Due to Proopiomelanocortin Deficiency: Three New Cases and Treatment Trials with Thyroid Hormone and ACTH4–10

The journal of clinical endocrinology and metabolism, 2003-10, Vol.88 (10), p.4633-4640

2003

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3-iodothyronamine differentially modulates α-2A-adrenergic receptor-mediated signaling

Journal of molecular endocrinology, 2015-06, Vol.54 (3), p.205-216

2015

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Update of the S2k guidelines : Surgical treatment of benign thyroid diseases

Chirurg, 2018-09, Vol.89 (9), p.699

2018

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A role for β-melanocyte-stimulating hormone in human body-weight regulation

Cell metabolism, 2006-02, Vol.3 (2), p.141-146

2006

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Analysis of the Wilms' Tumor Suppressor Gene (WT1) in Patients 46,XY Disorders of Sex Development

Thyroid dysfunction in pregnancy

Schilddrüsenerkrankungen im Kindes- und Jugendalter

Diagnostik seltener Erkrankungen in der Pädiatrie

Is there a further acceleration in the age at onset of menarche? A cross-sectional study in 1840 school children focusing on age and bodyweight at the onset of menarche

Metastabile Epiallele – beeinflussen epigenetische Varianten das individuelle Adipositasrisiko?

Development of a pediatric differentiated thyroid carcinoma registry within the EuRRECa project: rationale and protocol

Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis

No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency

Impaired glucose tolerance and type 2 diabetes mellitus: a new field for pediatrics in Europe

Two puzzling cases of thyroid dysgenesis

Treating patients not numbers: the benefit and burden of lowering TSH newborn screening cut-offs

Ethnicity and comorbidities in an overweight and obese multiethnic childhood cohort in Berlin

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency

Schilddrüsenhormon und Störungen des Zentralnervensystems

Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

Schilddrüsenfunktionsstörungen in der Schwangerschaft

Partielle Lipodystrophie mit Verdacht auf Autoimmunerkrankung

Consensus statement : Childhood obesity

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

Obesity Due to Proopiomelanocortin Deficiency: Three New Cases and Treatment Trials with Thyroid Hormone and ACTH4–10

3-iodothyronamine differentially modulates α-2A-adrenergic receptor-mediated signaling

Update of the S2k guidelines : Surgical treatment of benign thyroid diseases

A role for β-melanocyte-stimulating hormone in human body-weight regulation

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