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Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

The journal of clinical endocrinology and metabolism, 2008-11, Vol.93 (11), p.4183-4197

2008

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Long‐term follow‐up of female patients with congenital adrenal hyperplasia from 21‐hydroxylase deficiency, with special emphasis on the results of vaginoplasty

BJU international, 2000-08, Vol.86 (3), p.253-258

2000

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Functional and total IGFBP3 for the assessment of disorders of the GH/IGF1 axis in children with chronic kidney disease, GH deficiency, or short stature after SGA status at birth

European journal of endocrinology, 2012-05, Vol.166 (5), p.923-931

2012

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G.P.235

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.887-887

2014

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Low ovarian reserve in girls with autosomal-recessive proximal spinal muscular atrophies type I–III

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S196-S196

2015

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Association of Morphological Characteristics with Precocious Puberty and/or Gelastic Seizures in Hypothalamic Hamartoma

The journal of clinical endocrinology and metabolism, 2003-10, Vol.88 (10), p.4590-4595

2003

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Behavioural and emotional disturbances in people with Prader-Willi Syndrome

Journal of intellectual disability research, 2004-01, Vol.48 (1), p.47-52

2004

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Impact of overweight on effectiveness of treatment with human growth hormone in growth hormone deficient children: analysis of German KIGS data

Experimental and clinical endocrinology & diabetes, 2011-10, Vol.119 (9), p.544-548

2011

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Leydig Cell Hypoplasia: Absent Luteinizing Hormone Receptor Cell Surface Expression Caused by a Novel Homozygous Mutation in the Extracellular Domain

The journal of clinical endocrinology and metabolism, 2004-10, Vol.89 (10), p.5161-5167

2004

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Monitoring medical treatment in adolescents and young adults with congenital adrenal hyperplasia: utility of salivary 17α-hydroxyprogesterone day profiles

Experimental and clinical endocrinology & diabetes, 2011-03, Vol.119 (3), p.131-138

2011

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Glukokortikoide bei nichtendokrinen Erkrankungen, bei Kortisolmangel und bei endogenem Exzess – der Einfluss therapeutischer Strategien auf das kindliche Wachstum

Monatsschrift Kinderheilkunde, 2021-11, Vol.169 (11), p.1051-1058

2021

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Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001

European journal of endocrinology, 2002-11, Vol.147 (5), p.625-633

2002

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Long-term Surveillance of Children with Congenital Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (AQUAPE "Hypo Dok")

Klinische Padiatrie, 2015-07, Vol.227 (4), p.199

2015

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Male LH-Independent Sexual Precocity in a 3.5-Year-Old Boy Caused by a Somatic Activating Mutation of the LH Receptor in a Leydig Cell Tumor

The journal of clinical endocrinology and metabolism, 2002-03, Vol.87 (3), p.1052-1056

2002

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Microarray analysis reveals differential gene expression patterns and regulation of single target genes contributing to the opposing phenotype of TrkA- and TrkB-expressing neuroblastomas

Oncogene, 2005-01, Vol.24 (1), p.165-177

2005

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Why early surgery may not be enough: the search for new therapeutic strategies in cryptorchidism

Klinische Pädiatrie, 2008-09, Vol.220 (5), p.279

Hauffa, B P

2008

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Why Early Surgery May not be Enough: The Search for New Therapeutic Strategies in Cryptorchidism

Klinische Pädiatrie, 2008-09, Vol.220 (5), p.279-280

Hauffa, B.

2008

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Spontaneous growth in German children and adolescents with genetically confirmed Prader-Willi syndrome

Acta Paediatrica, 2000-11, Vol.89 (11), p.1302-1311

2000

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Casino gambling increases heart rate and salivary cortisol in regular gamblers

Biological psychiatry (1969), 2000-11, Vol.48 (9), p.948-953

2000

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Mutations in the amino-terminal domain of the human androgen receptor may be associated with partial androgen insensitivity and impaired transactivation in vitro

Experimental and clinical endocrinology & diabetes, 2005-09, Vol.113 (8), p.457-463

2005

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Management of adolescents with childhood onset growth hormone deficiency in the transition--results of a field based study in Germany

Deutsche medizinische Wochenschrift (1946), 2009-12, Vol.134 (50), p.2551

2009

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Male LH-Independent Sexual Precocity in a 3.5-Year-Old Boy Caused by a Somatic Activating Mutation of the LH Receptor in a Leydig Cell Tumor

The journal of clinical endocrinology and metabolism, 2002-03, Vol.87 (3), p.1052-1056

2002

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One-year results of growth hormone treatment of short stature in Prader-Willi syndrome

Acta Paediatrica, 1997-11, Vol.86 (S423), p.63-65

Hauffa, BP

1997

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Dehydroepiandrosterone Sulphate and Corticotropin Levels Are High in Young Male Patients with Conduct Disorder: Comparisons for Growth Factors, Thyroid and Gonadal Hormones

Neuropsychobiology, 2001-01, Vol.43 (3), p.134-140

2001

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Malformationen des Zentralnervensystems: Seltene Ursachen eines organischen Wachstumshormonmangels bei Kindern

Monatsschrift Kinderheilkunde, 2020-03, Vol.168 (3), p.246-251

2020

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Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

Long‐term follow‐up of female patients with congenital adrenal hyperplasia from 21‐hydroxylase deficiency, with special emphasis on the results of vaginoplasty

Functional and total IGFBP3 for the assessment of disorders of the GH/IGF1 axis in children with chronic kidney disease, GH deficiency, or short stature after SGA status at birth

G.P.235

Low ovarian reserve in girls with autosomal-recessive proximal spinal muscular atrophies type I–III

Association of Morphological Characteristics with Precocious Puberty and/or Gelastic Seizures in Hypothalamic Hamartoma

Behavioural and emotional disturbances in people with Prader-Willi Syndrome

Impact of overweight on effectiveness of treatment with human growth hormone in growth hormone deficient children: analysis of German KIGS data

Leydig Cell Hypoplasia: Absent Luteinizing Hormone Receptor Cell Surface Expression Caused by a Novel Homozygous Mutation in the Extracellular Domain

Monitoring medical treatment in adolescents and young adults with congenital adrenal hyperplasia: utility of salivary 17α-hydroxyprogesterone day profiles

Glukokortikoide bei nichtendokrinen Erkrankungen, bei Kortisolmangel und bei endogenem Exzess – der Einfluss therapeutischer Strategien auf das kindliche Wachstum

Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001

Long-term Surveillance of Children with Congenital Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (AQUAPE "Hypo Dok")

Male LH-Independent Sexual Precocity in a 3.5-Year-Old Boy Caused by a Somatic Activating Mutation of the LH Receptor in a Leydig Cell Tumor

Microarray analysis reveals differential gene expression patterns and regulation of single target genes contributing to the opposing phenotype of TrkA- and TrkB-expressing neuroblastomas

Why early surgery may not be enough: the search for new therapeutic strategies in cryptorchidism

Why Early Surgery May not be Enough: The Search for New Therapeutic Strategies in Cryptorchidism

Spontaneous growth in German children and adolescents with genetically confirmed Prader-Willi syndrome

Casino gambling increases heart rate and salivary cortisol in regular gamblers

Mutations in the amino-terminal domain of the human androgen receptor may be associated with partial androgen insensitivity and impaired transactivation in vitro

Management of adolescents with childhood onset growth hormone deficiency in the transition--results of a field based study in Germany

Male LH-Independent Sexual Precocity in a 3.5-Year-Old Boy Caused by a Somatic Activating Mutation of the LH Receptor in a Leydig Cell Tumor

One-year results of growth hormone treatment of short stature in Prader-Willi syndrome

Dehydroepiandrosterone Sulphate and Corticotropin Levels Are High in Young Male Patients with Conduct Disorder: Comparisons for Growth Factors, Thyroid and Gonadal Hormones

Malformationen des Zentralnervensystems: Seltene Ursachen eines organischen Wachstumshormonmangels bei Kindern

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