These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 3587632)

  • 1. Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy.
    Hart ZH; Servidei S; Peterson PL; Chang CH; DiMauro S
    Neurology; 1987 Jun; 37(6):1065-8. PubMed ID: 3587632
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy. Abnormal MRI findings in the head.
    Kashio N; Usuki F; Akamine T; Nakagawa S; Higuchi I; Nakahara K; Okada A; Osame M; Murata F
    J Neurol Sci; 1991 Sep; 105(1):1-5. PubMed ID: 1795162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Features of a syndrome with congenital cataract and hypertrophic cardiomyopathy.
    Cruysberg JR; Sengers RC; Pinckers A; Kubat K; van Haelst UJ
    Am J Ophthalmol; 1986 Dec; 102(6):740-9. PubMed ID: 3789054
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy.
    Bergia B; Sybers HD; Butler IJ
    J Neurol Neurosurg Psychiatry; 1986 Dec; 49(12):1423-6. PubMed ID: 3806120
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multicore myopathy: not always a benign entity.
    Shuaib A; Martin JM; Mitchell LB; Brownell AK
    Can J Neurol Sci; 1988 Feb; 15(1):10-4. PubMed ID: 3345455
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case report: lysosomal glycogen storage disease with normal acid maltase: an unusual form of hypertrophic cardiomyopathy with rapidly progressive heart failure.
    Tse HF; Shek TW; Tai YT; Lau YK; Ma L
    Am J Med Sci; 1996 Oct; 312(4):182-6. PubMed ID: 8853067
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments.
    Muntoni F; Catani G; Mateddu A; Rimoldi M; Congiu T; Faa G; Marrosu MG; Cianchetti C; Porcu M
    Neuromuscul Disord; 1994 May; 4(3):233-41. PubMed ID: 7919971
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A case of myotubular myopathy with mental retardation].
    Shikura K; Hokazono Y; Yoshizawa K
    No To Hattatsu; 1988 May; 20(3):247-8. PubMed ID: 3390366
    [No Abstract]   [Full Text] [Related]  

  • 9. [Centronuclear myopathy].
    Olivé M; Ferrer I; Jauma S; Montero J; Martínez-Matos JA
    Neurologia; 1993 Mar; 8(3):122-4. PubMed ID: 8448042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heteroplasmic mitochondrial DNA 3310 mutation in NADH dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation in a single patient.
    Hattori Y; Nakajima K; Eizawa T; Ehara T; Koyama M; Hirai T; Fukuda Y; Kinoshita M
    Diabetes Care; 2003 Mar; 26(3):952-3. PubMed ID: 12610069
    [No Abstract]   [Full Text] [Related]  

  • 11. Association of myopathy with multiple exostoses and mental retardation: a case report.
    De Stefano N; Dotti MT; Malandrini A; Federico A
    Brain Dev; 1994; 16(2):136-8. PubMed ID: 8048702
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A syndrome with juvenile cataract, cerebellar atrophy, mental retardation and myopathy.
    Herva R; von Wendt L; von Wendt G; Saukkonen AL; Leisti J; Dubowitz V
    Neuropediatrics; 1987 Aug; 18(3):164-9. PubMed ID: 3683758
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy.
    Murakami N; Goto Y; Itoh M; Katsumi Y; Wada T; Ozawa E; Nonaka I
    Neuromuscul Disord; 1995 Mar; 5(2):149-55. PubMed ID: 7539316
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mental retardation in congenital nonprogressive myopathy with uniform type 1 fibers.
    Jong YJ; Huang SC; Liu GC; Chiang CH
    Brain Dev; 1991 Nov; 13(6):444-6. PubMed ID: 1810161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).
    Nishino I; Fu J; Tanji K; Yamada T; Shimojo S; Koori T; Mora M; Riggs JE; Oh SJ; Koga Y; Sue CM; Yamamoto A; Murakami N; Shanske S; Byrne E; Bonilla E; Nonaka I; DiMauro S; Hirano M
    Nature; 2000 Aug; 406(6798):906-10. PubMed ID: 10972294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variants in NAA15 cause pediatric hypertrophic cardiomyopathy.
    Ritter A; Berger JH; Deardorff M; Izumi K; Lin KY; Medne L; Ahrens-Nicklas RC
    Am J Med Genet A; 2021 Jan; 185(1):228-233. PubMed ID: 33103328
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy.
    Amit R; Gutman A; Udassin R; Barash V; Kohn G
    Pediatr Neurol; 1988; 4(5):301-4. PubMed ID: 3242534
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Disease model: LAMP-2 enlightens Danon disease.
    Saftig P; Tanaka Y; Lüllmann-Rauch R; von Figura K
    Trends Mol Med; 2001 Jan; 7(1):37-9. PubMed ID: 11427988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A patient with lysosomal glycogen storage disease with normal acid maltase].
    Itoh M; Asano Y; Shimohira M; Iwakawa Y; Goto Y; Nonaka I
    No To Hattatsu; 1993 Sep; 25(5):459-64. PubMed ID: 8398237
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.