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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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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

2012

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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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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

2011

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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

2002

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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

2011

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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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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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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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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

2005

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Sexual precocity and recurrent β-human chorionic gonadotropin upsurges preceding the diagnosis of a malignant mediastinal germ-cell tumor in a 9-year-old boy

Annals of oncology, 2002-06, Vol.13 (6), p.975-977

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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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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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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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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Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1999-05, Vol.84 (5), p.1628-1632

1999

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Adiposity indices in German children and adolescents with genetically confirmed Prader-Willi syndrome (PWS)

International Journal of Obesity, 2001-05, Vol.25 Suppl 1 (S1), p.S22-S25

2001

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McCune-Albright syndrome--the German experience

Journal of pediatric endocrinology & metabolism : JPEM, 2002, Vol.15 Suppl 3, p.897

2002

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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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Growth retardation in Turner syndrome: Aneuploidy, rather than specific gene loss, may explain growth failure

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4578-4582

1999

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Hypothyroidism mimicking chronic renal failure in reflux nephropathy

Archives of disease in childhood, 2000-09, Vol.83 (3), p.251-252

2000

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Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

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

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

Behavioural and emotional disturbances in people with Prader-Willi Syndrome

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

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

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

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

Spontaneous growth in German children and adolescents with genetically confirmed 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

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

Sexual precocity and recurrent β-human chorionic gonadotropin upsurges preceding the diagnosis of a malignant mediastinal germ-cell tumor in a 9-year-old boy

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

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

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

Casino gambling increases heart rate and salivary cortisol in regular gamblers

Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia

Adiposity indices in German children and adolescents with genetically confirmed Prader-Willi syndrome (PWS)

McCune-Albright syndrome--the German experience

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

Growth retardation in Turner syndrome: Aneuploidy, rather than specific gene loss, may explain growth failure

Hypothyroidism mimicking chronic renal failure in reflux nephropathy

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