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 *

84 related articles for article (PubMed ID: 8711352)

  • 1. [Adult lysosomal and peroxisomal enzyme diseases and glycogenoses. I. Enzyme diseases with predominant symptoms in the fields of internal medicine, dermatology, orthopedics and ophthalmology].
    Elleder M
    Sb Lek; 1994; 95(3):221-30. PubMed ID: 8711352
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Adult lysosomal and peroxisomal enzyme diseases and glycogenoses. II. Enzyme diseases with predominant psychiatric and neurologic symptoms].
    Elleder M
    Sb Lek; 1994; 95(3):231-8. PubMed ID: 8711353
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Adult-onset metabolic diseases].
    García Ribes A; Martínez González M; García Cazorla A
    An Sist Sanit Navar; 2008; 31 Suppl 2():75-89. PubMed ID: 18953373
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mass spectrometry in the study of lysosomal storage disorders.
    Meikle PJ; Fuller M; Hopwood JJ
    Cell Mol Biol (Noisy-le-grand); 2003 Jul; 49(5):769-77. PubMed ID: 14528914
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inborn Errors of Metabolism Involving Complex Molecules: Lysosomal and Peroxisomal Storage Diseases.
    Bellettato CM; Hubert L; Scarpa M; Wangler MF
    Pediatr Clin North Am; 2018 Apr; 65(2):353-373. PubMed ID: 29502918
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New concepts in the diagnosis and treatment of lysosomal and peroxisomal disorders.
    Moser HW
    Curr Opin Neurol Neurosurg; 1992 Jun; 5(3):355-8. PubMed ID: 1623264
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan.
    Koto Y; Sakai N; Lee Y; Kakee N; Matsuda J; Tsuboi K; Shimozawa N; Okuyama T; Nakamura K; Narita A; Kobayashi H; Uehara R; Nakamura Y; Kato K; Eto Y
    Mol Genet Metab; 2021 Jul; 133(3):277-288. PubMed ID: 34090759
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lysosomal storage diseases as differential diagnoses to rheumatic disorders.
    Michels H; Mengel E
    Curr Opin Rheumatol; 2008 Jan; 20(1):76-81. PubMed ID: 18281861
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Lysosomal storage diseases for physicians: diagnosis and treatment].
    Ida H
    Rinsho Ketsueki; 2007 Oct; 48(10):1428-9. PubMed ID: 17933130
    [No Abstract]   [Full Text] [Related]  

  • 10. Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseases.
    Kopitz J; Harzer K; Kohlschütter A; Zöller B; Blenck N; Cantz M
    Am J Med Genet; 1996 May; 63(1):198-202. PubMed ID: 8723110
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early-onset lysosomal glycogen storage disease with normal acid maltase.
    Dayan RM; Renaud DL
    J Inherit Metab Dis; 2001 Aug; 24(4):504-6. PubMed ID: 11596653
    [No Abstract]   [Full Text] [Related]  

  • 12. Skin biopsy: a useful tool in the diagnosis of lysosomal storage diseases.
    Alroy J; Ucci AA
    Ultrastruct Pathol; 2006; 30(6):489-503. PubMed ID: 17182441
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Nation-wide survey on muscle glycogen storage disease (MGSDs) and comparison with our experiences in diagnosis of MGSDs].
    Fukuda T; Sugie H; Ito M; Sugie Y; Saito K; Nishino I; Shimizu T
    Rinsho Shinkeigaku; 2003 May; 43(5):243-8. PubMed ID: 12931628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Optic neuropathies in inherited metabolic disorders.
    Huizing M; Brooks BP; Anikster Y
    Pediatr Endocrinol Rev; 2005 Dec; 3(2):97-103. PubMed ID: 16361983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Systematic approach to the diagnosis of lysosomal storage disorders.
    Weibel TD; Brady RO
    Ment Retard Dev Disabil Res Rev; 2001; 7(3):190-9. PubMed ID: 11553935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hydrops fetalis: lysosomal storage disorders in extremis.
    Stone DL; Sidransky E
    Adv Pediatr; 1999; 46():409-40. PubMed ID: 10645471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases.
    Ramsay SL; Maire I; Bindloss C; Fuller M; Whitfield PD; Piraud M; Hopwood JJ; Meikle PJ
    Mol Genet Metab; 2004 Nov; 83(3):231-8. PubMed ID: 15542394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Newborn screening for lysosomal storage disorders.
    Meikle PJ; Ranieri E; Ravenscroft EM; Hua CT; Brooks DA; Hopwood JJ
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():104-10. PubMed ID: 11400743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurological manifestations in lysosomal storage disorders - from pathology to first therapeutic possibilities.
    Hoffmann B; Mayatepek E
    Neuropediatrics; 2005 Oct; 36(5):285-9. PubMed ID: 16217702
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Systemic diseases associated with retinal dystrophies.
    Werdich XQ; Place EM; Pierce EA
    Semin Ophthalmol; 2014; 29(5-6):319-28. PubMed ID: 25325857
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.