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Mariarosaria Lang-Muritano

Showing results (1-10 of 26) with videos related to

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Molecular and Cellular Endocrinology|July 5, 2022
Estrogens: Two nuclear receptors, multiple possibilitiesAnna Biason-Lauber, Mariarosaria Lang-Muritano
Pediatric Diabetes|March 12, 2008
Improved glycemic control and lower frequency of severe hypoglycemia with insulin detemir; long-term experience in 105 children and adolescents with type 1 diabetesDoris Braun, Daniel Konrad, Mariarosaria Lang-Muritano, et al.
Frontiers in Pediatrics|March 17, 2017
Two Siblings with the Same Severe Form of 21-Hydroxylase Deficiency But Different Growth and Menstrual Cycle PatternsMariarosaria Lang-Muritano, Karine Gerster, Susanna Sluka, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 5, 2019
A novel GATA6 variant in a boy with neonatal diabetes and diaphragmatic hernia: a familial case with a review of the literatureOdile Gaisl, Daniel Konrad, Pascal Joset, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2019
Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case reportZerin Sasivari, Gabor Szinnai, Britta Seebauer, et al.
Diabetes|June 28, 2002
Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 geneAnna Biason-Lauber, Mariarosaria Lang-Muritano, Tindara Vaccaro, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 12, 2022
Atypical familial diabetes associated with a novel <i>NEUROD1</i> nonsense variantJulia Mührer, Mariarosaria Lang-Muritano, Roger Lehmann, et al.
Pediatric Diabetes|July 24, 2012
Transient severe non-proliferative retinopathy in an adolescent with type 1 diabetes and chronic myeloid leukemiaSilvia Schmid, Mariarosaria Lang-Muritano, Urs Meier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 17, 2018
Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2)Mariarosaria Lang-Muritano, Patrick Sproll, Sascha Wyss, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2021
Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and BeyondTobias Troger, Grit Sommer, Mariarosaria Lang-Muritano, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Endocrinology|July 5, 2022
Estrogens: Two nuclear receptors, multiple possibilitiesAnna Biason-Lauber, Mariarosaria Lang-Muritano
Pediatric Diabetes|March 12, 2008
Improved glycemic control and lower frequency of severe hypoglycemia with insulin detemir; long-term experience in 105 children and adolescents with type 1 diabetesDoris Braun, Daniel Konrad, Mariarosaria Lang-Muritano, et al.
Frontiers in Pediatrics|March 17, 2017
Two Siblings with the Same Severe Form of 21-Hydroxylase Deficiency But Different Growth and Menstrual Cycle PatternsMariarosaria Lang-Muritano, Karine Gerster, Susanna Sluka, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 5, 2019
A novel GATA6 variant in a boy with neonatal diabetes and diaphragmatic hernia: a familial case with a review of the literatureOdile Gaisl, Daniel Konrad, Pascal Joset, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2019
Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case reportZerin Sasivari, Gabor Szinnai, Britta Seebauer, et al.
Diabetes|June 28, 2002
Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 geneAnna Biason-Lauber, Mariarosaria Lang-Muritano, Tindara Vaccaro, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 12, 2022
Atypical familial diabetes associated with a novel <i>NEUROD1</i> nonsense variantJulia Mührer, Mariarosaria Lang-Muritano, Roger Lehmann, et al.
Pediatric Diabetes|July 24, 2012
Transient severe non-proliferative retinopathy in an adolescent with type 1 diabetes and chronic myeloid leukemiaSilvia Schmid, Mariarosaria Lang-Muritano, Urs Meier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 17, 2018
Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2)Mariarosaria Lang-Muritano, Patrick Sproll, Sascha Wyss, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2021
Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and BeyondTobias Troger, Grit Sommer, Mariarosaria Lang-Muritano, et al.
Pageof 3