168 related articles for article (PubMed ID: 25965631)
1. Adverse clinical course and poor prognosis of hypertrophic cardiomyopathy due to mutations in FHL1.
Gallego-Delgado M; Gonzalez-Lopez E; Garcia-Guereta L; Ortega-Molina M; Gonzalez-Vioque E; Cobo-Marcos M; Alonso-Pulpon L; Garcia-Pavia P
Int J Cardiol; 2015 Jul; 191():194-7. PubMed ID: 25965631
[No Abstract] [Full Text] [Related]
2. X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene.
D'Arcy C; Kanellakis V; Forbes R; Wilding B; McGrath M; Howell K; Ryan M; McLean C
J Child Neurol; 2015 Aug; 30(9):1211-7. PubMed ID: 25246303
[TBL] [Abstract][Full Text] [Related]
3. Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene.
Hartmannova H; Kubanek M; Sramko M; Piherova L; Noskova L; Hodanova K; Stranecky V; Pristoupilova A; Sovova J; Marek T; Maluskova J; Ridzon P; Kautzner J; Hulkova H; Kmoch S
Circ Cardiovasc Genet; 2013 Dec; 6(6):543-51. PubMed ID: 24114807
[TBL] [Abstract][Full Text] [Related]
4. Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW; Wilding BR; Reischmann S; Crocini C; Lang P; Charron P; Müller OJ; McGrath MJ; Vollert I; Hansen A; Linke WA; Hengstenberg C; Bonne G; Morner S; Wichter T; Madeira H; Arbustini E; Eschenhagen T; Mitchell CA; Isnard R; Carrier L
Hum Mol Genet; 2012 Jul; 21(14):3237-54. PubMed ID: 22523091
[TBL] [Abstract][Full Text] [Related]
5. Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy - a case report.
Giucă A; Mitu C; Popescu BO; Bastian AE; Capşa R; Mursă A; Rădoi V; Popescu BA; Jurcuţ R
BMC Med Genet; 2020 Sep; 21(1):188. PubMed ID: 32993534
[TBL] [Abstract][Full Text] [Related]
6. Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy.
Gaertner-Rommel A; Tiesmeier J; Jakob T; Strickmann B; Veit G; Bachmann-Mennenga B; Paluszkiewicz L; Klingel K; Schulz U; Laser KT; Karger B; Pfeiffer H; Milting H
Mol Genet Genomic Med; 2019 Aug; 7(8):e841. PubMed ID: 31293105
[TBL] [Abstract][Full Text] [Related]
7. Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.
Knoblauch H; Geier C; Adams S; Budde B; Rudolph A; Zacharias U; Schulz-Menger J; Spuler A; Yaou RB; Nürnberg P; Voit T; Bonne G; Spuler S
Ann Neurol; 2010 Jan; 67(1):136-40. PubMed ID: 20186852
[TBL] [Abstract][Full Text] [Related]
8. Skeletal muscle biopsy analysis in reducing body myopathy and other FHL1-related disorders.
Malfatti E; Olivé M; Taratuto AL; Richard P; Brochier G; Bitoun M; Gueneau L; Laforêt P; Stojkovic T; Maisonobe T; Monges S; Lubieniecki F; Vasquez G; Streichenberger N; Lacène E; Saccoliti M; Prudhon B; Alexianu M; Figarella-Branger D; Schessl J; Bonnemann C; Eymard B; Fardeau M; Bonne G; Romero NB
J Neuropathol Exp Neurol; 2013 Sep; 72(9):833-45. PubMed ID: 23965743
[TBL] [Abstract][Full Text] [Related]
9. Description of a novel variant in the FHL1 gene associated with hypertrophic cardiomyopathy with early and aggressive presentation.
López Blázquez M; Fernández Ávila AI; Álvarez García-Rovés R; Centeno Jiménez M; Gómez González C; Espinosa Castro MÁ
Rev Esp Cardiol (Engl Ed); 2022 Nov; 75(11):968-970. PubMed ID: 35577730
[No Abstract] [Full Text] [Related]
10. Expanding the genetic spectrum of hypertrophic cardiomyopathy: X marks the spot.
Semsarian C; Ingles J
Circ Cardiovasc Genet; 2013 Dec; 6(6):528-30. PubMed ID: 24347617
[No Abstract] [Full Text] [Related]
11. Identification of a Novel Four and a Half LIM Domain 1 Mutation in a Chinese Male Presented with Hypertrophic Cardiomyopathy and Mild Skeletal Muscle Hypertrophy.
Zhang BQ; Si N; Liu DF
Chin Med J (Engl); 2015 Aug; 128(16):2269-70. PubMed ID: 26265627
[No Abstract] [Full Text] [Related]
12. Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
San Román I; Navarro M; Martínez F; Albert L; Polo L; Guardiola J; García-Molina E; Muñoz-Esparza C; López-Ayala JM; Sabater-Molina M; Gimeno JR
Clin Genet; 2016 Aug; 90(2):171-6. PubMed ID: 26857240
[TBL] [Abstract][Full Text] [Related]
13. Spongious hypertrophic cardiomyopathy in patients with mutations in the four-and-a-half LIM domain 1 gene.
Binder JS; Weidemann F; Schoser B; Niemann M; Machann W; Beer M; Plank G; Schmidt A; Bisping E; Poparic I; Lafer I; Stojakovic T; Quasthoff S; Vincent JB; Rienmueller R; Speicher MR; Berghold A; Pieske B; Windpassinger C
Circ Cardiovasc Genet; 2012 Oct; 5(5):490-502. PubMed ID: 22923418
[TBL] [Abstract][Full Text] [Related]
14. Selective muscle involvement in a family affected by a second LIM domain mutation of fhl1: an imaging study using computed tomography.
Komagamine T; Kawai M; Kokubun N; Miyatake S; Ogata K; Hayashi YK; Nishino I; Hirata K
J Neurol Sci; 2012 Jul; 318(1-2):163-7. PubMed ID: 22541254
[TBL] [Abstract][Full Text] [Related]
15. Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death.
Xue Y; Schoser B; Rao AR; Quadrelli R; Vaglio A; Rupp V; Beichler C; Nelson SF; Schapacher-Tilp G; Windpassinger C; Wilcox WR
Circ Cardiovasc Genet; 2016 Apr; 9(2):130-5. PubMed ID: 26933038
[TBL] [Abstract][Full Text] [Related]
16. Electrocardiographic analysis in unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
Peters S
Int J Cardiol; 2016 Jul; 214():136. PubMed ID: 27061647
[No Abstract] [Full Text] [Related]
17. FHL1-related myopathy may not be classified by reducing bodies in muscle biopsy.
Chen T; Lu X; Shi Q; Guo J; Wang H; Wang Q; Yin X; Zhang Y; Pu C; Zhou D
Neuromuscul Disord; 2020 Feb; 30(2):165-172. PubMed ID: 32001145
[TBL] [Abstract][Full Text] [Related]
18. Novel FHL1 mutation in a family with reducing body myopathy.
Schreckenbach T; Henn W; Kress W; Roos A; Maschke M; Feiden W; Dillmann U; Schulz JB; Weis J; Claeys KG
Muscle Nerve; 2013 Jan; 47(1):127-34. PubMed ID: 23169582
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 gene.
Sarkozy A; Windpassinger C; Hudson J; Dougan CF; Lecky B; Hilton-Jones D; Eagle M; Charlton R; Barresi R; Lochmüller H; Bushby K; Straub V
Eur J Hum Genet; 2011 Oct; 19(10):1038-44. PubMed ID: 21629301
[TBL] [Abstract][Full Text] [Related]
20. Reducing body myopathy and other FHL1-related muscular disorders.
Schessl J; Feldkirchner S; Kubny C; Schoser B
Semin Pediatr Neurol; 2011 Dec; 18(4):257-63. PubMed ID: 22172421
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]