Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Helmuth-G. Dörr"'
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 41-45 (2019)
Objective:Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion. There are a small number of reports in the literature showing higher birth weight and len
Externí odkaz:
https://doaj.org/article/ce525c9a34cc4a34b83ba7146b3c3156
Autor:
Helmuth G. Dörr, Theresa Penger, Michaela Marx, Manfred Rauh, Patricia G. Oppelt, Thomas K. M. Völkl
Publikováno v:
BMC Endocrine Disorders, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Data on adrenarche and pubarche in girls with Turner syndrome (TS) are inconsistent in the literature. Methods The cohort consisted of 94 girls and young women with TS born between 1971 and 2001 (age range: 3.1–23.2 yrs.), who w
Externí odkaz:
https://doaj.org/article/8ee9ea21941442b2ba3ae52063afb832
Publikováno v:
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background The most common form of congenital adrenal hyperplasia is 21-hydroxylase deficiency (CAH). Both men and women with classic CAH have lower fertility rates than the general population, and an increased rate of miscarriages has been
Externí odkaz:
https://doaj.org/article/1ba2372474fc441dbee2433bd20d6018
Autor:
Theresa Penger, Andrea Albrecht, Michaela Marx, Daniel Stachel, Markus Metzler, Helmuth G Dörr
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2018)
We report on a boy of Albanian descent with the history of juvenile myelomonocytic leukemia (JMML). JMML was diagnosed at the age of 17 months and treated by hematopoietic stem cell transplantation (HSCT). At the age of 14.3 years, about 12 years aft
Externí odkaz:
https://doaj.org/article/fac295271ace439089139c4c2fde3d5e
Autor:
Helmuth G. Dörr, Hartmut A. Wollmann, Berthold P. Hauffa, Joachim Woelfle, on behalf of the German Society of Pediatric Endocrinology and Diabetology
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Adrenal crises in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) are life-threatening and have the potential to death. Methods A survey was performed among Paediatric Endocrinologists i
Externí odkaz:
https://doaj.org/article/f9c1337dd29341a2adde267abf19634c
Autor:
Heike Hoyer-Kuhn, Alexander J Eckert, Gerhard Binder, Walter Bonfig, Angelika Dübbers, Stefan Riedl, Joachim Woelfle, Helmuth G Dörr, Reinhard W Holl
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Context Treatment of children with classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is challenging. Linear growth and adult height are compromised according to recent publications. However, most of these data were obtai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0510d0f40bbfbc5167d1415b67e0546c
https://doi.org/10.1210/clinem/dgad307
https://doi.org/10.1210/clinem/dgad307
Autor:
Helmuth G. Dörr, Patricia G. Oppelt
Publikováno v:
Gynäkologische Endokrinologie. 18:123-128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::644ad0d9dc361e00dca5f371c41d8145
https://doi.org/10.1007/s10304-020-00303-4
https://doi.org/10.1007/s10304-020-00303-4
Autor:
Helmuth G. Dörr, Patricia G. Oppelt
Publikováno v:
Pädiatrie up2date. 14:263-275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d9ee49003cd929b147826abd7847a93
https://doi.org/10.1055/a-0591-3658
https://doi.org/10.1055/a-0591-3658
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 41-45 (2019)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Objective: Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion. There are a small number of reports in the literature showing higher birth weight and le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6aa9e00b5a1fbdfce7328e9abb2c13c
https://doaj.org/article/ce525c9a34cc4a34b83ba7146b3c3156
https://doaj.org/article/ce525c9a34cc4a34b83ba7146b3c3156
Publikováno v:
Monatsschrift Kinderheilkunde. 169:639-644
Der M. Basedow ist im Kindes- und Jugendalter selten. Die Diagnosekriterien sind klar definiert; die Therapiemodalitaten werden kontrovers diskutiert. Retrospektive Analyse von Therapie und Langzeitverlauf der Patienten, die in der endokrinologischen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c94183258e9256d6df7d8706b5213d1a
https://doi.org/10.1007/s00112-019-0650-3
https://doi.org/10.1007/s00112-019-0650-3