| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| C Kampmann, C M Wiethoff, C Martin, A Wenzel, R Kampmann, C Whybra, E Miebach, M Bec. Electrocardiographic signs of hypertrophy in fabry disease-associated hypertrophic cardiomyopathy. Acta paediatrica (Oslo, Norway : 1992). Supplement. vol 91. issue 439. 2003-05-23. PMID:12572838. |
we aimed to evaluate the utility of different electrocardiographic (ecg) parameters for assessing the degree and severity of hypertrophic cardiomyopathy in patients with fabry disease. |
2003-05-23 |
2023-08-12 |
Not clear |
| B Sachdev, P M Elliot. Isolated cardiac manifestations in Fabry disease: the UK experience. Acta paediatrica (Oslo, Norway : 1992). Supplement. vol 91. issue 439. 2003-05-23. PMID:12572839. |
at st george's hospital medical school, a national referral centre for hypertrophic cardiomyopathy in the uk, a study of 153 consecutively referred male patients revealed that 4% had fabry disease. |
2003-05-23 |
2023-08-12 |
Not clear |
| B Sachdev, P M Elliot. Isolated cardiac manifestations in Fabry disease: the UK experience. Acta paediatrica (Oslo, Norway : 1992). Supplement. vol 91. issue 439. 2003-05-23. PMID:12572839. |
all these patients had electrocardiographic (ecg) abnormalities, most of which were consistent with those found in patients with classic fabry disease: left ventricular hypertrophy, repolarization abnormalities and a prolonged qrs complex. |
2003-05-23 |
2023-08-12 |
Not clear |
| 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. |
fabry disease in patients with hypertrophic cardiomyopathy (hcm). |
2003-04-14 |
2023-08-12 |
Not clear |
| 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. |
unlike patients with the classical systemic fabry disease entity, who present with multiple organ involvement, patients with a cardiac variant of fabry disease are characterized mainly by myocardial hypertrophy. |
2003-04-14 |
2023-08-12 |
Not clear |
| 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. |
therefore, the cardiac variant of fabry disease may be defined as a cardiomyocytic storage disorder, thus, mimicking the clinical features of hypertrophic obstructive and especially non-obstructive cardiomyopathy. |
2003-04-14 |
2023-08-12 |
Not clear |
| 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 patients with unexplained left ventricular hypertrophy the diagnosis of a cardiac variant of fabry disease is performed by light- and electron microscopic evaluation of endomyocardial catheter biopsy specimens and/or serologic investigations (decreased activity of alpha-galactosidase a in plasma or leucocytes). |
2003-04-14 |
2023-08-12 |
Not clear |
| 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. |
several studies show that between 4% and 8% of unselected patients with the clinical features of hypertrophic non-obstructive cardiomyopathy have a cardiac variant of fabry disease. |
2003-04-14 |
2023-08-12 |
Not clear |
| 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 |