Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Theresa Penger"'
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:
William G. Wilson, Arif B. Ekici, Helen Cox, Bernt Popp, Shagufta Khan, Bettina Behring, Moritz Hebebrand, Regina Trollmann, André Reis, Theresa Penger, Steffen Uebe, Cornelia Kraus, Joachim Woelfle, Mandy Krumbiegel, Georgia Vasileiou, Shelley Towner, Elisabeth Bosch
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Context CPE encodes carboxypeptidase E, an enzyme that converts proneuropeptides and propeptide hormones to bioactive forms. It is widely expressed in the endocrine and central nervous system. To date, 4 individuals from 2 families with core clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeb8d04d2563be5f9553065bca7cbe27
https://doi.org/10.1210/clinem/dgab592
https://doi.org/10.1210/clinem/dgab592
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
Publikováno v:
Monatsschrift Kinderheilkunde. 168:442-445
Eine Schilddrusenektopie ist extrem selten. Man findet ektopes Schilddrusengewebe als Folge eines gestorten embryonalen Migrationsprozesses gewohnlich im Bereich von der Zunge bis zum Zwerchfell, wobei insbesondere die linguale und sublinguale Lokali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a100922edb0eaf43a07b94dff445d4b5
https://doi.org/10.1007/s00112-018-0564-5
https://doi.org/10.1007/s00112-018-0564-5
Autor:
Helmuth G. Dörr, Markus Metzler, Theresa Penger, Michaela Marx, Daniel Stachel, Andrea Albrecht
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2018)
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::be41fef4eb08b74d3ff3e24d49c5bccd
https://www.edmcasereports.com/articles/endocrinology-diabetes-and-metabolism-case-reports/10.1530/EDM-18-0034
https://www.edmcasereports.com/articles/endocrinology-diabetes-and-metabolism-case-reports/10.1530/EDM-18-0034
Autor:
Theresa Penger, Thomas K. M. Völkl, Patricia G. Oppelt, Manfred Rauh, Michaela Marx, Helmuth G. Dörr
Publikováno v:
BMC Endocrine Disorders, Vol 19, Iss 1, Pp 1-5 (2019)
BMC Endocrine Disorders
BMC Endocrine Disorders
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 were treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9639037aee349b7b4a7c3193e27b01b7
https://doi.org/10.1186/s12902-019-0333-z
https://doi.org/10.1186/s12902-019-0333-z