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Results of search for 'au:"Lang-Muritano, M"'
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Authors
Acierno, J
Balercia, G
Belville, C
Biason-Lauber, A
Bircher, A J
Boehm, B
Boscaro, M
Bruckner-Tuderman, L
Brun, T
Cassatella, D
DeCampo, C
Dommann-Scherrer, C
Duff, C
Dwyer, A A
Fallo, F
Lang-Muritano, M
Molinari, L
Rosa, S
Schoenle, E J
Torresani, T
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Topics
Adolescent
Adult
Animals
Blood Glucose
COS Cells
Child
Chlorocebus aethiops
Cryptorchidism
Diabetes Mellitus, Type 1
Female
Gonadal Dysgenesis, 46,XY
Humans
Infant
Male
Mutation
Phenotype
Steroid 17-alpha-Hydroxylase
blood
genetics
metabolism
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English
Your search returned 11 results.
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1.
A novel mutation inducing partial androgen-insensitivity syndrome with phenotypic diversity.
[electronic resource]
by
Gobet, R
Lang-Muritano, M
Stallmach, T
Biason-Lauber, A
Producer:
20150819
In:
BJU international
vol. 92 Suppl 3
Online resources:
Available from publisher's website
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2.
Epidermolysis bullosa junctionalis progressiva in three siblings.
[electronic resource]
by
Bircher, A J
Lang-Muritano, M
Pfaltz, M
Bruckner-Tuderman, L
Producer:
19930624
In:
The British journal of dermatology
vol. 128
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3.
Incidence of enteropathy-associated T-cell lymphoma in celiac disease: implications for children and adolescents with type 1 diabetes.
[electronic resource]
by
Lang-Muritano, M
Molinari, L
Dommann-Scherrer, C
Schueler, G
Schoenle, E J
Producer:
20040630
In:
Pediatric diabetes
vol. 3
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4.
A novel mutation in the anti-müllerian hormone gene as cause of persistent müllerian duct syndrome.
[electronic resource]
by
Lang-Muritano, M
Biason-Lauber, A
Gitzelmann, C
Belville, C
Picard, Y
Schoenle, E J
Producer:
20020221
In:
European journal of pediatrics
vol. 160
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5.
Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency.
[electronic resource]
by
Rosa, S
Steigert, M
Lang-Muritano, M
l'Allemand, D
Schoenle, E J
Biason-Lauber, A
Producer:
20100524
In:
Hormone research in paediatrics
vol. 73
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6.
Acute cataracts in newly diagnosed IDDM in five children and adolescents.
[electronic resource]
by
Lang-Muritano, M
La Roche, G R
Stevens, J L
Gloor, B R
Schoenle, E J
Producer:
19961011
In:
Diabetes care
vol. 18
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7.
A physiological mode of puberty induction in hypogonadal girls by low dose transdermal 17 beta-oestradiol.
[electronic resource]
by
Illig, R
DeCampo, C
Lang-Muritano, M R
Prader, A
Torresani, T
Werder, E A
Willi, U
Schenkel, L
Producer:
19910313
In:
European journal of pediatrics
vol. 150
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8.
Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity.
[electronic resource]
by
Biason-Lauber, A
Boehm, B
Lang-Muritano, M
Gauthier, B R
Brun, T
Wollheim, C B
Schoenle, E J
Producer:
20050920
In:
Diabetologia
vol. 48
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9.
Epidemiology of type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade.
[electronic resource]
by
Schoenle, E J
Lang-Muritano, M
Gschwend, S
Laimbacher, J
Mullis, P E
Torresani, T
Biason-Lauber, A
Molinari, L
Producer:
20010823
In:
Diabetologia
vol. 44
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10.
Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism.
[electronic resource]
by
Xu, C
Lang-Muritano, M
Phan-Hug, F
Dwyer, A A
Sykiotis, G P
Cassatella, D
Acierno, J
Mohammadi, M
Pitteloud, N
Producer:
20180418
In:
Clinical genetics
vol. 92
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11.
P450c17 deficiency: clinical and molecular characterization of six patients.
[electronic resource]
by
Rosa, S
Duff, C
Meyer, M
Lang-Muritano, M
Balercia, G
Boscaro, M
Topaloglu, A Kemal
Mioni, R
Fallo, F
Zuliani, L
Mantero, F
Schoenle, E J
Biason-Lauber, A
Producer:
20070510
In:
The Journal of clinical endocrinology and metabolism
vol. 92
Online resources:
Available from publisher's website
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