Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism
Xu, C., Lang‐Muritano, M., Phan‐Hug, F., Dwyer, A.A., Sykiotis, G.P., Cassatella, D., Acierno, J., Mohammadi, M., Pitteloud, N.
Published in Clinical genetics (01.08.2017)
Published in Clinical genetics (01.08.2017)
Get full text
Journal Article
A novel mutation inducing partial androgen–insensitivity syndrome with phenotypic diversity
GOBET, R., LANG‐MURITANO, M., STALLMACH, T., BIASON‐LAUBER, A.
Published in BJU international (01.12.2003)
Published in BJU international (01.12.2003)
Get full text
Journal Article
P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients
Rosa, S, Duff, C, Meyer, M, Lang-Muritano, M, Balercia, G, Boscaro, M, Kemal Topaloglu, A, Mioni, R, Fallo, F, Zuliani, L, Mantero, F, Schoenle, E. J, Biason-Lauber, A
Published in The journal of clinical endocrinology and metabolism (01.03.2007)
Published in The journal of clinical endocrinology and metabolism (01.03.2007)
Get full text
Journal Article
Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade
SCHOENLE, E. J, LANG-MURITANO, M, GSCHWEND, S, LAIMBACHER, J, MULLIS, P. E, TORRESANI, T, BIASON-LAUBER, A, MOLINARI, L
Published in Diabetologia (01.03.2001)
Published in Diabetologia (01.03.2001)
Get full text
Journal Article
Epidermolysis bullosa junctionalis progressiva in three siblings
Bircher, A J, Lang-Muritano, M, Pfaltz, M, Bruckner-Tuderman, L
Published in British journal of dermatology (1951) (01.04.1993)
Published in British journal of dermatology (1951) (01.04.1993)
Get more information
Journal Article
Reply to comment on: Biason-Lauber A, Boehm B, Lang-Muritano M et al. (2005) Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity. Diabetologia 48:900–905
Biason-Lauber, A., Boehm, B., Lang-Muritano, M., Gauthier, B. R., Brun, T., Wollheim, C. B., Schoenle, E. J.
Published in Diabetologia (01.10.2005)
Published in Diabetologia (01.10.2005)
Get full text
Journal Article
Acute cataracts in newly diagnosed IDDM in five children and adolescents
Lang-Muritano, M, La Roche, G R, Stevens, J L, Gloor, B R, Schoenle, E J
Published in Diabetes care (01.10.1995)
Published in Diabetes care (01.10.1995)
Get full text
Journal Article
Clinical, Genetic and Functional Characteristics of Three Novel CYP17A1 Mutations Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Rosa, S., Steigert, M., Lang-Muritano, M., l’Allemand, D., Schoenle, E.J., Biason-Lauber, A.
Published in Hormone research in paediatrics (01.03.2010)
Published in Hormone research in paediatrics (01.03.2010)
Get full text
Journal Article
A physiological mode of puberty induction in hypogonadal girls by low dose transdermal 17 beta-oestradiol
Illig, R, DeCampo, C, Lang-Muritano, M R, Prader, A, Torresani, T, Werder, E A, Willi, U, Schenkel, L
Published in European journal of pediatrics (01.12.1990)
Published in European journal of pediatrics (01.12.1990)
Get more information
Journal Article
Clinical, Genetic and Functional Characteristics of Three Novel CYP17A1 Mutations Causing Combined 17[alpha]-Hydroxylase/17,20-Lyase Deficiency
Rosa, S, Steigert, M, Lang-muritano, M, L'allemand, D, Schoenle, E J, Biason-lauber, A
Published in Hormone research in paediatrics (01.03.2010)
Published in Hormone research in paediatrics (01.03.2010)
Get full text
Journal Article
Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency
Rosa, S, Steigert, M, Lang-Muritano, M, l'Allemand, D, Schoenle, E J, Biason-Lauber, A
Published in Hormone research in paediatrics (2010)
Published in Hormone research in paediatrics (2010)
Get full text
Journal Article
Association of childhood type 1 diabetes mellitus with a variant of PAX4 : possible link to beta cell regenerative capacity. Commentary
TIEDGE, M, BIASON-LAUBER, A, BOEHM, B, LANG-MURITANO, M, GAUTHIER, B. R, BRUN, T, WOLLHEIM, C. B, SCHOENLE, E. J
Published in Diabetologia (2005)
Get full text
Published in Diabetologia (2005)
Journal Article
Importance of Genetic Diagnosis of DAX-1 Deficiency: Example from a Large, Multigenerational Family
Ostermann, Sandrine, Salvi, Roberto, Lang-Muritano, Mariarosaria, Voirol, Marie-Jeanne, Puttinger, Rudolf, Gaillard, Rolf C., Schoenle, Eugen, Pralong, François P.
Published in Hormone research (01.01.2006)
Published in Hormone research (01.01.2006)
Get full text
Journal Article
A novel mutation in the anti-müllerian hormone gene as cause of persistent müllerian duct syndrome
LANG-MURITANO, Mariarosaria, BIASON-LAUBER, Anna, GITZELMANN, Christopher, BELVILLE, Corinne, PICARD, Yves, SCHOENLE, Eugen J
Published in European journal of pediatrics (01.11.2001)
Published in European journal of pediatrics (01.11.2001)
Get full text
Journal Article
Incidence of enteropathy-associated T-cell lymphoma in celiac disease: implications for children and adolescents with type 1 diabetes: Enteropathy-associated lymphoma and diabetes
Lang-Muritano, M., Molinari, L., Dommann-Scherrer, C., Schueler, G., Schoenle, E. J.
Published in Pediatric diabetes (01.03.2002)
Published in Pediatric diabetes (01.03.2002)
Get full text
Journal Article