| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| G Beer, P Reinecke, H E Gabbert, W Hort, H Kuh. Fabry disease in patients with hypertrophic cardiomyopathy (HCM). Zeitschrift fur Kardiologie. vol 91. issue 12. 2003-04-14. PMID:12490989. |
in each patient with unexplained myocardial hypertrophy concealed myocardial storage disease, especially cardiac fabry disease has to be considered and should be ruled out or confirmed by endomyocardial catheter biopsy. |
2003-04-14 |
2023-08-12 |
Not clear |
| Andreas Perrot, Karl Josef Osterziel, Michael Beck, Rainer Dietz, Christoph Kampman. Fabry disease: focus on cardiac manifestations and molecular mechanisms. Herz. vol 27. issue 7. 2003-03-07. PMID:12439642. |
the isolated cardiac variant of fabry disease seems to be more common than previously thought: around 3-6% of male patients with left ventricular hypertrophy seem to suffer from this disease variant. |
2003-03-07 |
2023-08-12 |
Not clear |
| M Uchino, E Uyama, H Kawano, J Hokamaki, K Kugiyama, Y Murakami, H Yasue, M And. A histochemical and electron microscopic study of skeletal and cardiac muscle from a Fabry disease patient and carrier. Acta neuropathologica. vol 90. issue 3. 1996-01-19. PMID:8525810. |
histochemical and electron microscopic studies were performed in an attempt to clarify the muscle pathology in an 18-year-old man with fabry disease, showing proximal limb muscle atrophy, and his 52-year-old mother, who is a fabry carrier with hypertrophic cardiomyopathy. |
1996-01-19 |
2023-08-12 |
Not clear |
| Y Nagao, H Nakashima, Y Fukuhara, M Shimmoto, A Oshima, Y Ikari, Y Mori, H Sakuraba, Y Suzuk. Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase A. Clinical genetics. vol 39. issue 3. 1991-07-03. PMID:1645238. |
hypertrophic cardiomyopathy in late-onset variant of fabry disease with high residual activity of alpha-galactosidase a. |
1991-07-03 |
2023-08-11 |
Not clear |
| Y Nagao, H Nakashima, Y Fukuhara, M Shimmoto, A Oshima, Y Ikari, Y Mori, H Sakuraba, Y Suzuk. Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase A. Clinical genetics. vol 39. issue 3. 1991-07-03. PMID:1645238. |
a new variant form of fabry disease with hypertrophic cardiomyopathy of late onset is reported. |
1991-07-03 |
2023-08-11 |
Not clear |