132 related articles for article (PubMed ID: 38083936)
1. Exercise induced muscle weakness in a young adult: McArdle's disease unusual presentation.
Kalsoom H; Mukhtar H; Latif RK
J Pak Med Assoc; 2023 Dec; 73(12):2473-2475. PubMed ID: 38083936
[TBL] [Abstract][Full Text] [Related]
2. [Massive rhabdomyolysis revealing a McArdle disease].
Loupy A; Pouchot J; Hertig A; Bonnard G; Bouvard E; Rondeau E
Rev Med Interne; 2007 Jul; 28(7):501-3. PubMed ID: 17383055
[TBL] [Abstract][Full Text] [Related]
3. McArdle's disease presenting with asymmetric, late-onset arm weakness.
Wolfe GI; Baker NS; Haller RG; Burns DK; Barohn RJ
Muscle Nerve; 2000 Apr; 23(4):641-5. PubMed ID: 10716777
[TBL] [Abstract][Full Text] [Related]
4. [McArdle's disease without typical symptoms].
Watanabe M; Matsubara E; Amari M; Okamoto K; Hirai S
Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
[TBL] [Abstract][Full Text] [Related]
5. McArdle's disease: two clinical expressions in the same pedigree.
Papadimitriou A; Manta P; Divari R; Karabetsos A; Papadimitriou E; Bresolin N
J Neurol; 1990 Jul; 237(4):267-70. PubMed ID: 2391551
[TBL] [Abstract][Full Text] [Related]
6. A novel compound heterozygous mutation in PYGM gene associated with McArdle's disease.
Iacono S; Lupica A; Di Stefano V; Borgione E; Brighina F
Acta Myol; 2022 Mar; 41(1):37-40. PubMed ID: 35465342
[TBL] [Abstract][Full Text] [Related]
7. Unforeseen cardiac involvement in McArdle's disease.
Moustafa S; Patton DJ; Connelly MS
Heart Lung Circ; 2013 Sep; 22(9):769-71. PubMed ID: 23337261
[TBL] [Abstract][Full Text] [Related]
8. McArdle's disease with late-onset symptoms: case report and review of the literature.
Felice KJ; Schneebaum AB; Jones HR
J Neurol Neurosurg Psychiatry; 1992 May; 55(5):407-8. PubMed ID: 1602316
[TBL] [Abstract][Full Text] [Related]
9. [MCARDLE'S DISEASE AND PHYSICAL ACTIVITY - A MIXED BLESSING].
Nemet D; Eliakim A
Harefuah; 2021 Jun; 160(6):377-381. PubMed ID: 34160155
[TBL] [Abstract][Full Text] [Related]
10. McArdle's disease in childhood: report of a new case.
Roubertie A; Patte K; Rivier F; Pages AM; Maire I; Echenne B
Eur J Paediatr Neurol; 1998; 2(5):269-73. PubMed ID: 10726830
[TBL] [Abstract][Full Text] [Related]
11. McArdle's disease: a clinical review and case report.
Keel BR; Brit M
Tenn Med; 2013; 106(10):33, 37. PubMed ID: 24282836
[TBL] [Abstract][Full Text] [Related]
12. Masticatory muscle symptoms in a patient with McArdle's disease.
Thornhill MH
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1996 May; 81(5):544-6. PubMed ID: 8734699
[TBL] [Abstract][Full Text] [Related]
13. McArdle's disease presenting as unexplained dyspnea in a young woman.
Voduc N; Webb KA; D'Arsigny C; McBride I; O'Donnell DE
Can Respir J; 2004 Mar; 11(2):163-7. PubMed ID: 15045049
[TBL] [Abstract][Full Text] [Related]
14. Glycogen storage disease type V (Mc Ardle's disease): a report on three cases.
Krishnamoorthy N; Santosh V; Yasha TC; Mahadevan A; Shankar SK; Jethwani D; Taly AB; Bhanu K; Gayathri N
Neurol India; 2011; 59(6):884-6. PubMed ID: 22234204
[TBL] [Abstract][Full Text] [Related]
15. [McArdle's disease. Apropos of a case].
Yuste JR; Beloqui O; De la Peña A; Rodríguez-Rosado R; Monreal JI; Prósper F; Prieto J
Rev Med Univ Navarra; 1998; 42(1):29-33. PubMed ID: 10420954
[TBL] [Abstract][Full Text] [Related]
16. Myoglobinuria and skeletal muscle phosphorylase deficiency: report of a case of McArdle's disease.
Nixon JC; Hobbs WK; Greenblatt J
Can Med Assoc J; 1966 May; 94(19):977-85. PubMed ID: 4952390
[TBL] [Abstract][Full Text] [Related]
17. [McArdle's disease: a case report].
Levy JA; Gagioti SM; Cavalieri MJ; Pereira JR
Arq Neuropsiquiatr; 1980 Dec; 38(4):411-4. PubMed ID: 6937160
[TBL] [Abstract][Full Text] [Related]
18. McArdle's disease with non-insulin-dependent diabetes mellitus: the beneficial effects of hyperglycemia and hyperinsulinemia for exercise intolerance.
Yamauchi A; Amano K; Ichikawa Y; Nakamoto S; Takei I; Maruyama H; Kono N; Saruta T
Intern Med; 1996 May; 35(5):403-6. PubMed ID: 8797056
[TBL] [Abstract][Full Text] [Related]
19. Pharmacological and nutritional treatment for McArdle's disease (Glycogen Storage Disease type V).
Quinlivan R; Beynon RJ
Cochrane Database Syst Rev; 2004; (3):CD003458. PubMed ID: 15266486
[TBL] [Abstract][Full Text] [Related]
20. [Muscle phosphorylase deficiency in childhood. A case report].
Bruno C; Iester A; Bado M; Morreale G; Broda P; Minetti C; Cordone A; Cordone G
Minerva Pediatr; 1994 Oct; 46(10):459-62. PubMed ID: 7808367
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]