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 *

80 related articles for article (PubMed ID: 8316526)

  • 1. The mucolipidoses.
    Gilbert-Barness EF; Barness LA
    Perspect Pediatr Pathol; 1993; 17():148-84. PubMed ID: 8316526
    [No Abstract]   [Full Text] [Related]  

  • 2. Prenatal diagnosis of mucolipidosis II--electron microscopy and biochemical evaluation.
    Carey WF; Jaunzems A; Richardson M; Fong BA; Chin SJ; Nelson PV
    Prenat Diagn; 1999 Mar; 19(3):252-6. PubMed ID: 10210124
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The inborn errors of sialic acid metabolism and their laboratory investigation.
    Gopaul KP; Crook MA
    Clin Lab; 2006; 52(3-4):155-69. PubMed ID: 16584062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosis.
    Falik-Zaccai TC; Zeigler M; Bargal R; Bach G; Borochowitz Z; Raas-Rothschild A
    Prenat Diagn; 2003 Mar; 23(3):211-4. PubMed ID: 12627421
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of microvillus inclusion disease.
    Chen CP; Su YN; Chern SR; Wu PC; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):399-400. PubMed ID: 22030065
    [No Abstract]   [Full Text] [Related]  

  • 6. Detection of chromosome aberrations during prenatal genetic testing for single gene disorders.
    Chen CP; Lin SP
    Prenat Diagn; 2004 Nov; 24(11):924-5. PubMed ID: 15565556
    [No Abstract]   [Full Text] [Related]  

  • 7. Cytochemical analysis of storage materials in cultured skin fibroblasts from patients with I-cell disease.
    Kawashima I; Ohsawa M; Fukushige T; Nagayama Y; Niida Y; Kotani M; Tajima Y; Kanekura T; Kanzaki T; Sakuraba H
    Clin Chim Acta; 2007 Mar; 378(1-2):142-6. PubMed ID: 17204262
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electron microscopy of cultured skin fibroblasts and amniotic fluid cells in the diagnosis of hereditary storage diseases.
    Ornoy A; Sekeles E; Cohen R; Kohn G
    Monogr Hum Genet; 1978; 10():32-9. PubMed ID: 102925
    [No Abstract]   [Full Text] [Related]  

  • 9. [Degradation of glycoconjugates in lysosomes and its disorders].
    Itoh K; Sakuraba H
    Tanpakushitsu Kakusan Koso; 1992 Aug; 37(11 Suppl):1951-6. PubMed ID: 1410488
    [No Abstract]   [Full Text] [Related]  

  • 10. The mucopolysaccharidoses and mucolipidoses as model systems for the investigation of genetic disorders.
    Shapiro LJ
    Birth Defects Orig Artic Ser; 1981; 17(2):191-203. PubMed ID: 6461367
    [No Abstract]   [Full Text] [Related]  

  • 11. [Inborn errors of lysosome protease].
    Katunuma N; Kominami E
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):715-7. PubMed ID: 3270886
    [No Abstract]   [Full Text] [Related]  

  • 12. Distinguishing Pacman dysplasia from mucolipidosis II: comment on Saul et al. [2005].
    Wilcox WR; Wenger DA; Lachman RS; Rimoin DL
    Am J Med Genet A; 2005 Jun; 135(3):333. PubMed ID: 15887286
    [No Abstract]   [Full Text] [Related]  

  • 13. [Biochemical diagnosis of lysosomal storage diseases in medico-genetic centers. I. Mucopolysaccharidoses, mucolipidoses (review of the literature)].
    Gusina NB; Tsukerman GL
    Lab Delo; 1990; (8):12-8. PubMed ID: 1705591
    [No Abstract]   [Full Text] [Related]  

  • 14. Early prenatal diagnosis of mucolipidosis IV.
    Ornoy A; Arnon J; Grebner EE; Jackson LG; Bach G
    Am J Med Genet; 1987 Aug; 27(4):983-5. PubMed ID: 3425607
    [No Abstract]   [Full Text] [Related]  

  • 15. Mucolipidosis IV.
    Cantani A
    Am J Dis Child; 1983 Jan; 137(1):88. PubMed ID: 6847966
    [No Abstract]   [Full Text] [Related]  

  • 16. The missing link in lysosomal enzyme targeting.
    Sly WS
    J Clin Invest; 2000 Mar; 105(5):563-4. PubMed ID: 10712426
    [No Abstract]   [Full Text] [Related]  

  • 17. [Mucolipidosis: clinical and genetic aspects].
    Kolodny EH
    Rev Neurol; 1998 Aug; 27(156):337-41. PubMed ID: 9736966
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel missense mutations in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes.
    Itoh K; Naganawa Y; Matsuzawa F; Aikawa S; Doi H; Sasagasako N; Yamada T; Kira J; Kobayashi T; Pshezhetsky AV; Sakuraba H
    J Hum Genet; 2002; 47(1):29-37. PubMed ID: 11829139
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [I-cell disease and pseudo-Hurler polydystrophy].
    Owada M
    Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):475-9. PubMed ID: 11031999
    [No Abstract]   [Full Text] [Related]  

  • 20. [Familial mucolipidosis type II (I-cell disease)].
    Stopyrowa J; Pietrzyk JA; Fyderek K; Spodaryk M; Barylak A; Miezyński W; Kaczmarski F
    Pol Tyg Lek; 1988 Sep; 43(39):1256-9. PubMed ID: 3244584
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.