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Lang-Muritano, Mariarosaria
43
results:
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Online (43)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (21)
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1
Defective jagged-1 signaling affects GnRH development and c..:
Cotellessa, Ludovica
;
Marelli, Federica
;
Duminuco, Paolo
...
JCI Insight. 8 (2023) 5 - p. , 2023
Link:
https://doi.org/10.1172/..
?
2
Estrogens: Two nuclear receptors, multiple possibilities:
Biason-Lauber, Anna
;
Lang-Muritano, Mariarosaria
Molecular and Cellular Endocrinology. 554 (2022) - p. 111710 , 2022
Link:
https://doi.org/10.1016/..
?
3
Aktuelle Herausforderungen in der Therapie des Typ-1-Diabet..:
Boettcher, Claudia
;
Burckardt, Marie-Anne
;
Heldt, Kathrin
...
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum. , 2022
Link:
https://doi.org/10.4414/..
?
4
Défis actuels dans le traitement du diabète de type 1 chez ..:
Boettcher, Claudia
;
Burckardt, Marie-Anne
;
Heldt, Kathrin
...
Forum Médical Suisse ‒ Swiss Medical Forum. , 2022
Link:
https://doi.org/10.4414/..
?
5
Characteristics of Growth in Children With Classic Congenit..:
Troger, Tobias
;
Sommer, Grit
;
Lang-Muritano, Mariarosaria
...
The Journal of Clinical Endocrinology & Metabolism. 107 (2021) 2 - p. e487-e499 , 2021
Link:
https://doi.org/10.1210/..
?
6
Loss-of-function and missense variants in NSD2 cause decrea..:
Zanoni, Paolo
;
Steindl, Katharina
;
Sengupta, Deepanwita
...
Genetics in Medicine. 23 (2021) 8 - p. 1474-1483 , 2021
Link:
https://doi.org/10.1038/..
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7
Pathogenic mosaic variants in congenital hypogonadotropic h..:
Acierno, James S.
;
Xu, Cheng
;
Papadakis, Georgios E.
...
Genetics in Medicine. 22 (2020) 11 - p. 1759-1767 , 2020
Link:
https://doi.org/10.1038/..
?
8
Congenital hypogonadotropic hypogonadism and constitutional..:
Cassatella, Daniele
;
Howard, Sasha R
;
Acierno, James S
...
European Journal of Endocrinology. 178 (2018) 4 - p. 377-388 , 2018
Link:
https://doi.org/10.1530/..
?
9
Early-Onset Complete Ovarian Failure and Lack of Puberty in..:
Lang-Muritano, Mariarosaria
;
Sproll, Patrick
;
Wyss, Sascha
...
The Journal of Clinical Endocrinology & Metabolism. 103 (2018) 10 - p. 3748-3756 , 2018
Link:
https://doi.org/10.1210/..
?
10
Two Siblings with the Same Severe Form of 21-Hydroxylase De..:
Lang-Muritano, Mariarosaria
;
Gerster, Karine
;
Sluka, Susanna
.
Frontiers in Pediatrics. 5 (2017) - p. , 2017
Link:
https://doi.org/10.3389/..
?
11
DCC/NTN1 complex mutations in patients with congenital hypo..:
Bouilly, Justine
;
Messina, Andrea
;
Papadakis, Georgios
...
Human Molecular Genetics. 27 (2017) 2 - p. 359-372 , 2017
Link:
https://doi.org/10.1093/..
?
12
When Genetic Load Does Not Correlate with Phenotypic Spectr..:
Gianetti, Elena
;
Hall, Janet E.
;
Au, Margaret G.
...
The Journal of Clinical Endocrinology & Metabolism. 97 (2012) 9 - p. E1798-E1807 , 2012
Link:
https://doi.org/10.1210/..
?
13
Aromatase Deficiency in Fetal Virilization:
Stalberg, Katharina
;
Gonzales, Ricardo
;
Lang-Muritano, Mariarosaria
.
Journal of Pediatric Urology. 6 (2010) - p. S85 , 2010
Link:
https://doi.org/10.1016/..
?
14
Clinical, Genetic, and Functional Characterization of Four ..:
Sahakitrungruang, Taninee
;
Soccio, Raymond E.
;
Lang-Muritano, Mariarosaria
...
The Journal of Clinical Endocrinology & Metabolism. 95 (2010) 7 - p. 3352-3359 , 2010
Link:
https://doi.org/10.1210/..
?
15
GNRH1 Mutations in Patients with Idiopathic Hypogonadotropi..:
Chan, Yee-Ming
;
de Guillebon, Adelaide
;
Lang-Muritano, Mariarosaria
...
Proceedings of the National Academy of Sciences of the United States of America. 106 (2009) 28 - p. 11703-11708 , 2009
Link:
https://www.jstor.org/st..
1-15