Strehle E[au] - Search Results

Year	Number of Results
2001	1
2003	2
2004	1
2006	1
2007	2
2008	3
2009	4
2010	2
2011	3
2012	5
2013	2
2014	1
2015	1
2018	1
2019	2
2022	0

1

New ways of preventing vitamin K deficiency bleeding in infancy.

Strehle EM. Strehle EM. Acta Paediatr. 2019 Nov;108(11):1936-1937. doi: 10.1111/apa.14945. Epub 2019 Sep 10. Acta Paediatr. 2019. PMID: 31502702 No abstract available.

2

Recent advances in the management of Duchenne muscular dystrophy.

Strehle EM, Straub V. Strehle EM, et al. Arch Dis Child. 2015 Dec;100(12):1173-7. doi: 10.1136/archdischild-2014-307962. Epub 2015 Jul 7. Arch Dis Child. 2015. PMID: 26153505 Review.

3

The phenotype of patients with 4q-syndrome.

Strehle EM, Bantock HM. Strehle EM, et al. Genet Couns. 2003;14(2):195-205. Genet Couns. 2003. PMID: 12872814 Review.

4

The 4q-Syndrome.

Strehle EM, Ahmed OA, Hameed M, Russell A. Strehle EM, et al. Genet Couns. 2001;12(4):327-39. Genet Couns. 2001. PMID: 11837601

5

Long-term management of children with neuromuscular disorders.

Strehle EM. Strehle EM. J Pediatr (Rio J). 2009 Sep-Oct;85(5):379-84. doi: 10.2223/JPED.1929. J Pediatr (Rio J). 2009. PMID: 19830355 Review. English, Portuguese.

6

Sialic acid storage disease and related disorders.

Strehle EM. Strehle EM. Genet Test. 2003 Summer;7(2):113-21. doi: 10.1089/109065703322146795. Genet Test. 2003. PMID: 12885332 Review.

7

Dysferlinopathy: from gene to protein.

Strehle EM. Strehle EM. J Clin Neuromuscul Dis. 2008 Dec;10(2):83-4. doi: 10.1097/CND.0b013e3181873cb8. J Clin Neuromuscul Dis. 2008. PMID: 19169097 No abstract available.

8

Can home monitoring reduce mortality in infants at increased risk of sudden infant death syndrome? A systematic review.

Strehle EM, Gray WK, Gopisetti S, Richardson J, McGuire J, Malone S. Strehle EM, et al. Acta Paediatr. 2012 Jan;101(1):8-13. doi: 10.1111/j.1651-2227.2011.02464.x. Epub 2011 Oct 10. Acta Paediatr. 2012. PMID: 21910748 Review.

9

Assessing prevalence of alcohol consumption in early pregnancy: Self-report compared to blood biomarker analysis.

Howlett H, Mackenzie S, Gray WK, Rankin J, Nixon L, Richardson A, Strehle EM, Brown NW. Howlett H, et al. Among authors: strehle em. Eur J Med Genet. 2018 Sep;61(9):531-538. doi: 10.1016/j.ejmg.2018.05.009. Eur J Med Genet. 2018. PMID: 29753916

10

Dysmorphological and pharmacological studies in 4q- syndrome.

Strehle EM. Strehle EM. Genet Couns. 2011;22(2):173-85. Genet Couns. 2011. PMID: 21848010

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