Lang-Muritano M - Search Results

1

Children with congenital hypothyroidism: long-term intellectual outcome after early high-dose treatment.

Dimitropoulos A, Molinari L, Etter K, Torresani T, Lang-Muritano M, Jenni OG, Largo RH, Latal B. Dimitropoulos A, et al. Pediatr Res. 2009 Feb;65(2):242-8. doi: 10.1203/PDR.0b013e31818d2030. Pediatr Res. 2009. PMID: 18787501

2

A physiological mode of puberty induction in hypogonadal girls by low dose transdermal 17 beta-oestradiol.

Illig R, DeCampo C, Lang-Muritano MR, Prader A, Torresani T, Werder EA, Willi U, Schenkel L. Illig R, et al. Eur J Pediatr. 1990 Dec;150(2):86-91. doi: 10.1007/BF02072044. Eur J Pediatr. 1990. PMID: 2126236

3

Epidemiology of type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade.

Schoenle EJ, Lang-Muritano M, Gschwend S, Laimbacher J, Mullis PE, Torresani T, Biason-Lauber A, Molinari L. Schoenle EJ, et al. Diabetologia. 2001 Mar;44(3):286-9. doi: 10.1007/s001250051615. Diabetologia. 2001. PMID: 11317657

4

Incidence of enteropathy-associated T-cell lymphoma in celiac disease: implications for children and adolescents with type 1 diabetes.

Lang-Muritano M, Molinari L, Dommann-Scherrer C, Schueler G, Schoenle EJ. Lang-Muritano M, et al. Pediatr Diabetes. 2002 Mar;3(1):42-5. doi: 10.1034/j.1399-5448.2002.30108.x. Pediatr Diabetes. 2002. PMID: 15016174

5

Improved glycemic control and lower frequency of severe hypoglycemia with insulin detemir; long-term experience in 105 children and adolescents with type 1 diabetes.

Braun D, Konrad D, Lang-Muritano M, Schoenle E. Braun D, et al. Pediatr Diabetes. 2008 Aug;9(4 Pt 2):382-7. doi: 10.1111/j.1399-5448.2008.00371.x. Epub 2008 Mar 5. Pediatr Diabetes. 2008. PMID: 18331413

6

Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case report.

Sasivari Z, Szinnai G, Seebauer B, Konrad D, Lang-Muritano M. Sasivari Z, et al. Among authors: lang muritano m. J Pediatr Endocrinol Metab. 2019 Nov 26;32(11):1299-1303. doi: 10.1515/jpem-2019-0051. J Pediatr Endocrinol Metab. 2019. PMID: 31541602 Free article.

7

Transient severe non-proliferative retinopathy in an adolescent with type 1 diabetes and chronic myeloid leukemia.

Schmid S, Lang-Muritano M, Meier U, De Peron R, Konrad D, Schoenle E. Schmid S, et al. Pediatr Diabetes. 2013 May;14(3):227-9. doi: 10.1111/j.1399-5448.2012.00901.x. Epub 2012 Jul 23. Pediatr Diabetes. 2013. PMID: 22817266

8

Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes.

Stekelenburg C, Gerster K, Blouin JL, Lang-Muritano M, Guipponi M, Santoni F, Schwitzgebel VM. Stekelenburg C, et al. Pediatr Diabetes. 2019 May;20(3):366-369. doi: 10.1111/pedi.12814. Epub 2019 Feb 17. Pediatr Diabetes. 2019. PMID: 30684292

9

A novel GATA6 variant in a boy with neonatal diabetes and diaphragmatic hernia: a familial case with a review of the literature.

Gaisl O, Konrad D, Joset P, Lang-Muritano M. Gaisl O, et al. J Pediatr Endocrinol Metab. 2019 Sep 25;32(9):1027-1030. doi: 10.1515/jpem-2019-0057. J Pediatr Endocrinol Metab. 2019. PMID: 31271559 Free article. Review.

10

Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and Beyond.

Troger T, Sommer G, Lang-Muritano M, Konrad D, Kuhlmann B, Zumsteg U, Flück CE. Troger T, et al. Among authors: lang muritano m. J Clin Endocrinol Metab. 2022 Jan 18;107(2):e487-e499. doi: 10.1210/clinem/dgab701. J Clin Endocrinol Metab. 2022. PMID: 34599587 Free PMC article.

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