Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Lutz, Wünsch"'
Autor:
Judith Lindert, Tina Straube, Beke Larsen, Julia Siebert, Eirini Liodaki, Kianusch Tafazzoli-Lari, Lutz Wünsch
Publikováno v:
European Burn Journal, Vol 5, Iss 2, Pp 155-165 (2024)
To define the morphologic pattern of pediatric hand burns as visualized via optical coherence tomography (OCT) and dynamic OCT (D-OCT). We designed a scoring system to assess the depths of burn wounds on pediatric hands and tested this score in our c
Externí odkaz:
https://doaj.org/article/f2856dd93a8644599987049fe80e8725
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 7, Iss C, Pp 28-30 (2016)
The turban pin inhalation syndrome is known as a subtype of foreign body aspiration, mainly occurring in girls and young women wearing turbans. With the number of turban wearing girls and women increasing all over the world, attention must be brought
Externí odkaz:
https://doaj.org/article/6e5db2938116438b8cf427ffda94b1c6
Autor:
Ralf Werner, Isabel Mönig, Ralf Lünstedt, Lutz Wünsch, Christoph Thorns, Benedikt Reiz, Alexandra Krause, Karl Otfried Schwab, Gerhard Binder, Paul-Martin Holterhus, Olaf Hiort
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176720 (2017)
Mutations in NR5A1 have been reported as a frequent cause of 46,XY disorders of sex development (DSD) associated to a broad phenotypic spectrum ranging from infertility, ambiguous genitalia, anorchia to gonadal dygenesis and female genitalia. Here we
Externí odkaz:
https://doaj.org/article/835aba8029de45f995189961ff0d0c36
Autor:
Verónica Calonga-Solís, Helena Fabbri-Scallet, Fabian Ott, Mostafa Al-Sharkawi, Axel Künstner, Lutz Wünsch, Olaf Hiort, Hauke Busch, Ralf Werner
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 16; Pages: 4858
De novo variants in the myelin regulatory factor (MYRF), a transcription factor involved in the differentiation of oligodendrocytes, have been linked recently to the cardiac and urogenital syndrome, while familiar variants are associated with nanopht
Publikováno v:
Der Chirurg. 92:189-193
Endoskopische Diagnostik und Interventionen bei Kindern erfordern ein hohes Mas an Expertise aus unterschiedlichen Bereichen. Die kleinen Dimensionen, die Vulnerabilitat der Patienten*innen und die Seltenheit der Erkrankungen und Problematiken einers
Publikováno v:
Gynäkologische Endokrinologie. 19:38-45
Storungen, Besonderheiten oder Varianten der Geschlechtsentwicklung („differences of sex development“, DSD) bezeichnen eine Gruppe von Menschen mit angeborenen Diskrepanzen zwischen chromosomalem, gonadalem und phanotypischem Geschlecht. Diagnost
Publikováno v:
Pädiatrie & Pädologie. 56:15-23
Storungen, Besonderheiten oder Varianten der Geschlechtsentwicklung („differences of sex development“, DSD) bezeichnen eine Gruppe von Menschen mit angeborenen Diskrepanzen zwischen chromosomalem, gonadalem und phanotypischem Geschlecht. Diagnost
Autor:
Isabel Mönig, Olaf Hiort, Anders Juul, Ralf Werner, Louise Marshall, Ralf Lünstedt, Wiebke Birnbaum, Julia Schneidewind, Lutz Wünsch, Trine Holm Johannsen
Publikováno v:
Mönig, I, Schneidewind, J, Johannsen, T H, Juul, A, Werner, R, Lünstedt, R, Birnbaum, W, Marshall, L, Wünsch, L & Hiort, O 2022, ' Pubertal development in 46,XY patients with NR5A1 mutations ', Endocrine, vol. 75, no. 2, pp. 601-613 . https://doi.org/10.1007/s12020-021-02883-y
Purpose Mutations in the NR5A1 gene, encoding the transcription factor Steroidogenic Factor-1, are associated with a highly variable genital phenotype in patients with 46,XY differences of sex development (DSD). Our objective was to analyse the puber
Publikováno v:
Der Chirurg; Zeitschrift fur alle Gebiete der operativen MedizenLiteratur. 92(3)
Endoscopic diagnostics and interventions in children require a high level of expertise from different fields. The small dimensions, the vulnerability of the patients and the rarity of the diseases and problems as well as the necessity for the most mo
Autor:
H. Stoop, Mirian Yumie Nishi, Lutz Wünsch, J. W. Oosterhuis, Ad J. M. Gillis, Katja P. Wolffenbuttel, J Kaprová, Sorahia Domenice, Martine Cools, Charmian A. Quigley, Remko Hersmus, Berenice B. Mendonca, Guy T'Sjoen, Stenvert L. S. Drop, Leendert H. J. Looijenga, Elaine Maria Frade Costa
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Human Reproduction, 32(12), 2561-2573. Oxford University Press
Universidade de São Paulo (USP)
instacron:USP
Human Reproduction, 32(12), 2561-2573. Oxford University Press
STUDY QUESTION: What is the prevalence of malignant testicular germ cell tumors (TGCT) and its precursors, (pre-) germ cell neoplasia in situ (GCNIS), in late teenagers and adults who have androgen insensitivity syndrome (AIS) and the impact of an in