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 *

81 related articles for article (PubMed ID: 672028)

  • 41. Neutral lipid storage disease with ichthyosis. Defective lamellar body contents and intracellular dispersion.
    Elias PM; Williams ML
    Arch Dermatol; 1985 Aug; 121(8):1000-8. PubMed ID: 4026335
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Ichthyosis with neutral lipid storage: Dorfman-Chanarin syndrome. Apropos of a familial case].
    Venencie PY; Pauwels C; Rekik A; Mielot F; Hadchouel M; Odievre M
    Ann Dermatol Venereol; 1993; 120(11):758-60. PubMed ID: 8210101
    [No Abstract]   [Full Text] [Related]  

  • 43. [Ocular myopathies with mitochondrial abnormalities. Apropos of 4 cases with histological and ultrastructural study of the ocular muscle in 2 cases].
    Saraux H; Offret H; Nou B; Mikol J
    Bull Soc Ophtalmol Fr; 1974 Mar; 74(3):305-17. PubMed ID: 4468128
    [No Abstract]   [Full Text] [Related]  

  • 44. [Features of disorders of carbohydrate metabolism in progressive muscular dystrophies (review)].
    Badalian LO; Temin PA; Ametov AS; Khasanova KhD; Il'in IL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(3):122-6. PubMed ID: 6344519
    [No Abstract]   [Full Text] [Related]  

  • 45. [Genetic diseases of lipid storage and related disorders].
    Künnert B
    Zentralbl Pathol; 1992 Jun; 138(3):168-208. PubMed ID: 1525132
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Screening for Duchenne muscular dystrophy.
    Roses AD; Nicholson GA; Roe CR
    Pediatrics; 1977 Aug; 60(2):248-51. PubMed ID: 887342
    [No Abstract]   [Full Text] [Related]  

  • 47. [Lipid peroxidation in children with Duchenne's hereditary myopathy].
    Grinio LP; Orlov ON; Prilipko LL; Kagan VE
    Biull Eksp Biol Med; 1984 Oct; 98(10):423-5. PubMed ID: 6498321
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Round table conference: clinical aspect of myopathy].
    Toyokura Y; Kase M; Sugita H; Ebashi S; Satoyoshi E
    Naika; 1970 Apr; 25(4):694-710. PubMed ID: 5423423
    [No Abstract]   [Full Text] [Related]  

  • 49. [On progressive myopathy with muscle phosphorylase deficiency and giant mitochondria].
    Sluga E; Seitelberger F; Moser K
    Wien Klin Wochenschr; 1967 Dec; 79(49):917-21. PubMed ID: 4231954
    [No Abstract]   [Full Text] [Related]  

  • 50. Inborn errors of lipid metabolism. Familial hyperlipoproteinaemia type 3. Detection of heterozygotes.
    Sobra J; Heyrovský A
    Rev Czech Med; 1972; 18(1):34-9. PubMed ID: 5022312
    [No Abstract]   [Full Text] [Related]  

  • 51. Late onset of neutral lipid storage disease due to a rare PNPLA2 mutation in a patient with myopathy and cardiomyopathy.
    Tian Y; Wang S; Wang F; Yi L; Dong M; Huang X
    Chin Med J (Engl); 2022 Oct; 135(19):2389-2391. PubMed ID: 36535014
    [No Abstract]   [Full Text] [Related]  

  • 52. Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason.
    Kleefeld F; von Renesse A; Dittmayer C; Harms L; Radke J; Radbruch H; Goebel HH; Pache F; Schneider U; Schuelke M; Uruha A; Stenzel W
    Neuropathol Appl Neurobiol; 2022 Feb; 48(1):e12731. PubMed ID: 33969514
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Disturbances of amino acid metabolism in clinical syndromes not characterised by a primary amino acidopathy.
    Bremer HJ; Przyrembel H
    Clin Endocrinol Metab; 1974 Mar; 3(1):131-43. PubMed ID: 4609644
    [No Abstract]   [Full Text] [Related]  

  • 54. Respiration rate of muscle mitochondria from genetically dystrophic chickens.
    March BE; Biely J; Coates V
    Proc Soc Exp Biol Med; 1968 Nov; 129(2):566-8. PubMed ID: 5701471
    [No Abstract]   [Full Text] [Related]  

  • 55. Infantile neuroaxonal dystrophy.
    Crome L; Weller SD
    Arch Dis Child; 1965 Oct; 40(213):502-7. PubMed ID: 5829994
    [No Abstract]   [Full Text] [Related]  

  • 56. Ranolazine-induced lipid storage myopathy presenting with respiratory failure and head drop.
    Paul P; Vazquez Do Campo R; Liewluck T; Naddaf E
    Neuromuscul Disord; 2021 Jun; 31(6):546-550. PubMed ID: 33903020
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Hereditary abnormalities in plasma lipids].
    Fuhrmann W
    Humangenetik; 1966; 2(1):1-20. PubMed ID: 5332664
    [No Abstract]   [Full Text] [Related]  

  • 58. Familial metabolic disorder with fatty metamorphosis of the viscera.
    Peremans J; De Graef PJ; Strubbe G; De Block G
    J Pediatr; 1966 Dec; 69(6):1108-12. PubMed ID: 5953838
    [No Abstract]   [Full Text] [Related]  

  • 59. [Early infantile malignant lipid storage myopathy].
    Hinkel GK; Kemmer C; Probsthain AR; Roschlau G; Todt H
    Kinderarztl Prax; 1978 May; 46(5):235-9. PubMed ID: 672028
    [No Abstract]   [Full Text] [Related]  

  • 60. [Unusual phenotype of myopathy associated with a new PNPLA2 mutation].
    Jousserand G; Streichenberger N; Petiot P
    Med Sci (Paris); 2016 Nov; 32 Hors série n°2():10-11. PubMed ID: 27869069
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.