J. Rohayem

发表

Age and markers of Leydig cell function, but not of Sertoli cell function predict the success of sperm retrieval in adolescents and adults with Klinefelter's syndrome

S. Kliesch, J. Wistuba, M. Zitzmann, 2015, Andrology.

German version of the Hypogonadism Impact of Symptoms Questionnaire: Psychometric properties and association with testosterone levels

Martina K. Schmidt, G. Schneider, H. Gelhorn, 2022, Andrologia.

Effects of adolescence-onset hypogonadism on metabolism, bone mineral density and quality of life in adulthood

Friederike I. Tam, L. Hofbauer, A. Huebner, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Delayed treatment of undescended testes may promote hypogonadism and infertility

E. Nieschlag, S. Kliesch, M. Zitzmann, 2017, Endocrine.

Collaboration for rare diabetes: understanding new treatment options for Wolfram syndrome

C. de Beaufort, T. Danne, A. Schwandt, 2021, Endocrine.

Central Hypogonadism in the Male: Physiopathology, Diagnosis and Treatment

E. Nieschlag, J. Rohayem, 2018 .

Causes of hypogonadotropic hypogonadism predict response to gonadotropin substitution in adults

E. Nieschlag, S. Kliesch, M. Zitzmann, 2016, Andrology.

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

V. Tillmann, P. Chanson, M. Dattani, 2020, Orphanet Journal of Rare Diseases.

Inhibin B, AMH, but not INSL3, IGF1 or DHEAS support differentiation between constitutional delay of growth and puberty and hypogonadotropic hypogonadism

E. Nieschlag, S. Kliesch, M. Zitzmann, 2015, Andrology.

Congenital Hypogonadotropic Hypogonadism and Kallmann's Syndrome

E. Nieschlag, M. Zitzmann, J. Rohayem, 2014 .

Diabetes and Neurodegeneration in Wolfram Syndrome

G. Salzano, O. Kordonouri, A. Huebner, 2011, Diabetes Care.

Testicular function in males with infantile nephropathic cystinosis

D. Haffner, S. Kliesch, S. Huss, 2021, Human reproduction.

Testicular function during puberty and young adulthood in patients with Klinefelter's syndrome with and without spermatozoa in seminal fluid

E. Nieschlag, S. Kliesch, M. Zitzmann, 2016, Andrology.

Development and evaluation of a patient education programme for children, adolescents, and young adults with differences of sex development (DSD) and their parents: study protocol of Empower-DSD

S. Roll, I. Menrath, O. Hiort, 2022, BMC Endocrine Disorders.

University of Birmingham EURO-WABB : an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome

V. Tillmann, S. Aymé, T. Barrett, 2013 .

Impact of various progestins with or without transdermal testosterone on gonadotropin levels for non‐invasive hormonal male contraception: a randomized clinical trial

E. Nieschlag, S. Kliesch, M. Zitzmann, 2017, Andrology.

Testicular growth and spermatogenesis: new goals for pubertal hormone replacement in boys with hypogonadotropic hypogonadism? ‐a multicentre prospective study of hCG/rFSH treatment outcomes during adolescence‐

M. Zacharin, S. Kliesch, B. Hauffa, 2017, Clinical endocrinology.

A history of undescended testes in young men with Klinefelter syndrome does not reduce the chances for successful microsurgical testicular sperm extraction

E. Nieschlag, S. Kliesch, M. Zitzmann, 2018, Andrology.

Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome

M. Zitzmann, J. Rohayem, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Restoration of fertility by gonadotropin replacement in a man with hypogonadotropic azoospermia and testicular adrenal rest tumors due to untreated simple virilizing congenital adrenal hyperplasia.

E. Nieschlag, S. Kliesch, M. Zitzmann, 2014, European journal of endocrinology.

Monogenic diabetes syndromes: Locus‐specific databases for Alström, Wolfram, and Thiamine‐responsive megaloblastic anemia

V. Tillmann, F. Urano, T. Hershey, 2017, Human mutation.

Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity‐onset diabetes of the young (MODY)

M. Gahr, A. Näke, A. Galler, 2005, Human Mutation.

Molecular Aging Markers in Patients with Klinefelter Syndrome

S. Kliesch, J. Gromoll, M. Zitzmann, 2019, Aging and disease.

Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement

A. Huebner, R. Pfaeffle, J. Rohayem, 2016, Hormone Research in Paediatrics.

The role of gonadotropins in testicular and adrenal androgen biosynthesis pathways—Insights from males with congenital hypogonadotropic hypogonadism on hCG/rFSH and on testosterone replacement

E. Nieschlag, S. Kliesch, M. Zitzmann, 2020, Clinical endocrinology.

EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome

Richard Sinnott, Véronique Paquis-Flucklinger, Kay Parkinson, 2013, BMC Pediatrics.

Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

P. Chanson, J. Bertherat, T. Battelino, 2022, European journal of endocrinology.

Gonadal function in adult male patients with congenital adrenal hyperplasia.

P. Span, F. Sweep, A. V. van Herwaarden, 2018, European journal of endocrinology.

Pulmonary fibrosis and other clinical manifestations of small vessel vasculitis in a family with seropositive juvenile rheumatoid arthritis

M. Gahr, W. Leupold, J. Rohayem, 2002, Pediatric pulmonology.

The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres

R. McGowan, A. Novelli, C. Gravholt, 2022, Endocrine connections.

Monogenic diabetes syndromes: Locusspecific databases for Alstrm, Wolfram, and Thiamineresponsive megaloblastic anemia

V. Tillmann, T. Hershey, P. Yu-Wai-Man, 2018 .

University of Birmingham Monogenic diabetes syndromes

T. Hershey, P. Yu-Wai-Man, L. Tranebjaerg, 2017 .

Testicular Architecture of Men with 46,XX Testicular Disorders of Sex Development

C. Gravholt, J. Wistuba, A. Berglund, 2023, Sexual Development.

Semen quality and testicular adrenal rest tumor development in 46,XY congenital adrenal hyperplasia - the importance of optimal hormonal replacement.

J. Weigel, S. Kliesch, F. Reschke, 2021, European journal of endocrinology.