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Lang-Muritano, Mariarosaria
46  results:
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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/..
 
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2

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/..
 
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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/..
 
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4

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/..
 
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5

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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6

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/..
 
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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/..
 
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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/..
 
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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/..
 
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10

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/..
 
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11

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/..
 
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12

Transient severe non-proliferative retinopathy in an adoles..:

Schmid, Silvia ; Lang-Muritano, Mariarosaria ; Meier, Urs...
Pediatric Diabetes.  , 2012
Link: https://doi.org/10.1111/..
 
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13

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/..
 
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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/..
 
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15

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/..
 
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