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 *

115 related articles for article (PubMed ID: 7211157)

  • 1. Familial centronuclear myopathy.
    Pavone L; Mollica F; Grasso A; Pero G
    Acta Neurol Scand; 1980 Jul; 62(1):33-40. PubMed ID: 7211157
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Autosomal dominant centronuclear myopathy].
    Ferrer X; Vital C; Coquet M; Deleplanque B; Ellie E; Lagueny A; Julien J
    Rev Neurol (Paris); 1992; 148(10):622-30. PubMed ID: 1295057
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Centronuclear myopathy with autosomal dominant inheritance.
    McLeod JG; Baker Wde C; Lethlean AK; Shorey CD
    J Neurol Sci; 1972 Apr; 15(4):375-87. PubMed ID: 5016690
    [No Abstract]   [Full Text] [Related]  

  • 4. [Centronuclear myopathy with autosomal dominant inheritance(author's transl)].
    Mortier W; Michaelis E; Becker J; Gerhard L
    Humangenetik; 1975; 27(3):199-215. PubMed ID: 1150240
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial congenital fiber type disproportion (CFTD) with an autosomal recessive inheritance.
    Jaffe M; Shapira J; Borochowitz Z
    Clin Genet; 1988 Jan; 33(1):33-7. PubMed ID: 3342545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Centronuclear myopathy in black African children--report of 4 cases.
    Moosa A; Dawood AA
    Neuropediatrics; 1987 Nov; 18(4):213-7. PubMed ID: 3696389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome.
    Jadro-Santel D; Grcević N; Dogan S; Franjić J; Benc H
    J Neurol Sci; 1980 Feb; 45(1):43-56. PubMed ID: 6244371
    [TBL] [Abstract][Full Text] [Related]  

  • 8. X-linked centronuclear myopathy as a cause of floppy baby.
    Donders G; Moerman P; Devlieger H; Spitz B; Van Assche FA
    Eur J Obstet Gynecol Reprod Biol; 1987 Jan; 24(1):33-8. PubMed ID: 3817270
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Centronuclear myopathy.
    Dugan G; Yngve DA
    Orthopedics; 1985 Aug; 8(8):1041, 1043. PubMed ID: 3832049
    [No Abstract]   [Full Text] [Related]  

  • 10. [Partial deficiency of cytochrome c oxidase in skeletal muscles; two cousins presenting progressive external ophthalmoplegia and proximal weakness of the limbs].
    Madarame H; Nomura T; Chiba K; Niitsu M; Sano M; Tohgi H
    Nihon Naika Gakkai Zasshi; 1987 Mar; 76(3):414-20. PubMed ID: 3039025
    [No Abstract]   [Full Text] [Related]  

  • 11. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea.
    Scrimgeour EM; Mastaglia FL
    Am J Med Genet; 1984 Apr; 17(4):763-71. PubMed ID: 6720743
    [TBL] [Abstract][Full Text] [Related]  

  • 12. VCP myopathy: A family with unusual clinical manifestations.
    Guo X; Zhao Z; Shen H; Qi B; Li N; Hu J
    Muscle Nerve; 2019 Mar; 59(3):365-369. PubMed ID: 30488450
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.
    Darin N; Kyllerman M; Wahlström J; Martinsson T; Oldfors A
    Ann Neurol; 1998 Aug; 44(2):242-8. PubMed ID: 9708547
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oculopharyngodistal myopathy.
    Satoyoshi E; Kinoshita M
    Arch Neurol; 1977 Feb; 34(2):89-92. PubMed ID: 836191
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial nemaline myopathy: case reports.
    Antoniades K; Taskos N; Mavromatis J; Sakkas L; Karakasis D
    Oral Surg Oral Med Oral Pathol; 1991 Jul; 72(1):51-4. PubMed ID: 1653926
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics of congenital nemaline myopathy: a study of 10 families.
    Wallgren-Pettersson C; Kääriäinen H; Rapola J; Salmi T; Jääskeläinen J; Donner M
    J Med Genet; 1990 Aug; 27(8):480-7. PubMed ID: 2213842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Oculopharyngeal myopathy with sensorineural hearing loss.
    Alusi GH; Grant WE; Quiney RE
    J Laryngol Otol; 1996 Jun; 110(6):567-9. PubMed ID: 8763380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Centronuclear myopathy: possible central nervous system origin.
    Serratrice G; Pellissier JF; Faugere MC; Gastaut JL
    Muscle Nerve; 1978; 1(1):62-9. PubMed ID: 752109
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A benign congenital myopathy in an inbred Samaritan family.
    Lev D; Sadeh M; Watemberg N; Dabby R; Vinkler C; Ginzberg M; Lerman-Sagie T
    Eur J Paediatr Neurol; 2006 Jul; 10(4):182-5. PubMed ID: 16959509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial form of centronuclear myopathy in the adult].
    Pépin B; Mikol J; Goldstein B; Haguenau M; Godlewski S
    Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.