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 *

210 related articles for article (PubMed ID: 8002065)

  • 1. Storage disorders presenting like mucopolysaccharidosis.
    Sanklecha MU; Kher A; Naik GG; Bharucha BA; Mahajan P
    Indian J Pediatr; 1994; 61(4):367-72. PubMed ID: 8002065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The mucopolysaccharidoses and related conditions.
    Eggli KD; Dorst JP
    Semin Roentgenol; 1986 Oct; 21(4):275-94. PubMed ID: 3097828
    [No Abstract]   [Full Text] [Related]  

  • 3. Tandem mass spectrometry-based multiplex assays for α-mannosidosis and fucosidosis.
    Kumar AB; Hong X; Yi F; Wood T; Gelb MH
    Mol Genet Metab; 2019 Jul; 127(3):207-211. PubMed ID: 31235216
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hereditary lysosomal diseases in Mexico. II. Laboratory diagnosis of mucopolysaccharidosis and mucolipidosis].
    Zetina ME; Gonzalez-Noriega A
    Rev Invest Clin; 1990; 42(3):165-73. PubMed ID: 2125355
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lysosomal storage in human skeletal muscle.
    Carpenter S; Karpati G
    Hum Pathol; 1986 Jul; 17(7):683-703. PubMed ID: 3087857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic mucopolysaccharidoses, mannosidosis, sialidosis, galactosialidosis, and I-cell disease. Ultrastructural analysis of cultured fibroblasts.
    Takahashi K; Naito M; Suzuki Y
    Acta Pathol Jpn; 1987 Mar; 37(3):385-400. PubMed ID: 3113172
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oligosaccharide analysis in urine by maldi-tof mass spectrometry for the diagnosis of lysosomal storage diseases.
    Xia B; Asif G; Arthur L; Pervaiz MA; Li X; Liu R; Cummings RD; He M
    Clin Chem; 2013 Sep; 59(9):1357-68. PubMed ID: 23676310
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High proportion of mannosidosis and fucosidosis among lysosomal storage diseases in Cuba.
    Menéndez-Sainz C; González-Quevedo A; González-García S; Peña-Sánchez M; Giugliani R
    Genet Mol Res; 2012 Aug; 11(3):2352-9. PubMed ID: 22911605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lysosomal storage diseases in Greece.
    Michelakakis H; Dimitriou E; Tsagaraki S; Giouroukos S; Schulpis K; Bartsocas CS
    Genet Couns; 1995; 6(1):43-7. PubMed ID: 7794561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. I Cell Disease (Mucolipidosis II Alpha/Beta): From Screening to Molecular Diagnosis.
    Singh A; Prasad R; Gupta AK; Sharma A; Alves S; Coutinho MF; Kapoor S; Mishra OP
    Indian J Pediatr; 2017 Feb; 84(2):144-146. PubMed ID: 27785713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A program of prevention of hereditary lysosomal diseases in the USSR].
    Krasnopol'skaia KD; Mirenburg TV; Aronovich EL; Lebedeva TV; Akhunov VS; Odinokova ON; Chebysheva MV; Demina NA; Nikiforova OK; Kuznetsov MI
    Vestn Ross Akad Med Nauk; 1992; (4):20-4. PubMed ID: 1384872
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Blood and bone marrow cytology in the diagnosis of illnesses of excess. Forty observations of mucopolysaccharidosis, mucolipidosis and mannosidosis].
    Cosson A; Maroteaux P; Tapon J; Maier M; Girot R
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):205-6. PubMed ID: 408792
    [No Abstract]   [Full Text] [Related]  

  • 13. [The mucopolysaccharidosis, mucolipidosis and lipidosis: their interrelationship and differential diagnosis (author's transl)].
    Chida N
    Rinsho Byori; 1976; 24(11):887-95. PubMed ID: 137996
    [No Abstract]   [Full Text] [Related]  

  • 14. Bony changes in common mucopolysaccharidoses.
    Chen SJ; Li YW; Wang TR; Hsu JC
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1996; 37(3):178-84. PubMed ID: 8755171
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Detection of mucopolysaccharidosis and mucolipidosis by quantitative and qualitative analyses of urinary complex carbohydrates].
    Ejiri M; Watanabe T; Ueta Y; Koseki M
    Rinsho Byori; 1983 Mar; 31(3):336-40. PubMed ID: 6223161
    [No Abstract]   [Full Text] [Related]  

  • 16. [Thin-layer chromatography of urine oligosaccharides in diagnosis of some lysosomal storage disorders].
    Lugowska A; Tylki-Szymańska A; Sawnor-Korszyńska D
    Pediatr Pol; 1995 Oct; 70(10):847-55. PubMed ID: 8649932
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of urinary oligosaccharide excretion patterns by UHPLC/HRAM mass spectrometry for screening of lysosomal storage disorders.
    Hagemeijer MC; van den Bosch JC; Bongaerts M; Jacobs EH; van den Hout JMP; Oussoren E; Ruijter GJG
    J Inherit Metab Dis; 2023 Mar; 46(2):206-219. PubMed ID: 36752951
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Radiological and clinical characterization of the lysosomal storage disorders: non-lipid disorders.
    Parker EI; Xing M; Moreno-De-Luca A; Harmouche E; Terk MR
    Br J Radiol; 2014 Jan; 87(1033):20130467. PubMed ID: 24234586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lysosomal storage disorders in Thailand: the Siriraj experience.
    Wasant P; Wattanaweeradej S; Raksadawan N; Kolodny EH
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():54-8. PubMed ID: 8629143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Lysosomal storage diseases].
    Manger B
    Z Rheumatol; 2010 Aug; 69(6):527-38. PubMed ID: 20532791
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.