Frohn-Mulder IM - Search Results

1

Effect of enzyme therapy in juvenile patients with Pompe disease: a three-year open-label study.

van Capelle CI, van der Beek NA, Hagemans ML, Arts WF, Hop WC, Lee P, Jaeken J, Frohn-Mulder IM, Merkus PJ, Corzo D, Puga AC, Reuser AJ, van der Ploeg AT. van Capelle CI, et al. Neuromuscul Disord. 2010 Dec;20(12):775-82. doi: 10.1016/j.nmd.2010.07.277. Neuromuscul Disord. 2010. PMID: 20817528 Clinical Trial.

2

Cardiac evaluation in children and adults with Pompe disease sharing the common c.-32-13T>G genotype rarely reveals abnormalities.

van der Beek NA, Soliman OI, van Capelle CI, Geleijnse ML, Vletter WB, Kroos MA, Reuser AJ, Frohn-Mulder IM, van Doorn PA, van der Ploeg AT. van der Beek NA, et al. J Neurol Sci. 2008 Dec 15;275(1-2):46-50. doi: 10.1016/j.jns.2008.07.013. Epub 2008 Aug 30. J Neurol Sci. 2008. PMID: 18757064

3

Mucopolysaccharidosis: cardiologic features and effects of enzyme-replacement therapy in 24 children with MPS I, II and VI.

Brands MM, Frohn-Mulder IM, Hagemans ML, Hop WC, Oussoren E, Helbing WA, van der Ploeg AT. Brands MM, et al. J Inherit Metab Dis. 2013 Mar;36(2):227-34. doi: 10.1007/s10545-011-9444-z. Epub 2012 Jan 26. J Inherit Metab Dis. 2013. PMID: 22278137 Free PMC article.

4

Cardiac outcome in classic infantile Pompe disease after 13 years of treatment with recombinant human acid alpha-glucosidase.

van Capelle CI, Poelman E, Frohn-Mulder IM, Koopman LP, van den Hout JMP, Régal L, Cools B, Helbing WA, van der Ploeg AT. van Capelle CI, et al. Among authors: frohn mulder im. Int J Cardiol. 2018 Oct 15;269:104-110. doi: 10.1016/j.ijcard.2018.07.091. Epub 2018 Jul 19. Int J Cardiol. 2018. PMID: 30049495 Free article.

5

Delayed Diagnosis of Danon Disease in Patients Presenting With Isolated Cardiomyopathy.

Demirdas S, van Slegtenhorst MA, Verdijk RM, Lee M, van den Hout HMP, Wessels MW, Frohn-Mulder IME, Gardeitchik T, van der Ploeg AT, Schaaf GJ. Demirdas S, et al. Among authors: frohn mulder ime. Circ Genom Precis Med. 2019 Mar;12(3):e002395. doi: 10.1161/CIRCGEN.118.002395. Circ Genom Precis Med. 2019. PMID: 30919683 No abstract available.

6

First locus for primary pulmonary vein stenosis maps to chromosome 2q.

van de Laar I, Wessels M, Frohn-Mulder I, Dalinghaus M, de Graaf B, van Tienhoven M, van der Moer P, Husen-Ebbinge M, Lequin M, Dooijes D, de Krijger R, Oostra BA, Bertoli-Avella AM. van de Laar I, et al. Eur Heart J. 2009 Oct;30(20):2485-92. doi: 10.1093/eurheartj/ehp271. Epub 2009 Jul 4. Eur Heart J. 2009. PMID: 19578166

7

Short- and midterm results of balloon valvuloplasty for valvular aortic stenosis in children.

Witsenburg M, Cromme-Dijkhuis AH, Frohn-Mulder IM, Hess J. Witsenburg M, et al. Am J Cardiol. 1992 Apr 1;69(9):945-50. doi: 10.1016/0002-9149(92)90798-4. Am J Cardiol. 1992. PMID: 1532286

8

Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.

Hoedemaekers YM, Cohen-Overbeek TE, Frohn-Mulder IM, Dooijes D, Majoor-Krakauer DF. Hoedemaekers YM, et al. Ultrasound Obstet Gynecol. 2013 Mar;41(3):336-9. doi: 10.1002/uog.12279. Ultrasound Obstet Gynecol. 2013. PMID: 22859017 Free article.

9

The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.

Hoedemaekers YM, Caliskan K, Michels M, Frohn-Mulder I, van der Smagt JJ, Phefferkorn JE, Wessels MW, ten Cate FJ, Sijbrands EJ, Dooijes D, Majoor-Krakauer DF. Hoedemaekers YM, et al. Circ Cardiovasc Genet. 2010 Jun;3(3):232-9. doi: 10.1161/CIRCGENETICS.109.903898. Epub 2010 Jun 8. Circ Cardiovasc Genet. 2010. PMID: 20530761

10

Management of fixed subaortic stenosis: a retrospective study of 57 cases.

de Vries AG, Hess J, Witsenburg M, Frohn-Mulder IM, Bogers JJ, Bos E. de Vries AG, et al. J Am Coll Cardiol. 1992 Apr;19(5):1013-7. doi: 10.1016/0735-1097(92)90286-v. J Am Coll Cardiol. 1992. PMID: 1532402 Free article.

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