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 *

130 related articles for article (PubMed ID: 4529697)

  • 1. [Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)].
    Schaub J; Osang M; von Bassewitz DB; Grote W; Terinde R; Lombeck I; Bremer HJ
    Dtsch Med Wochenschr; 1974 Nov; 99(44):2219-22, 27. PubMed ID: 4529697
    [No Abstract]   [Full Text] [Related]  

  • 2. [Type II glycogenosis].
    Joram A; Fessard C; Tron P; de Menibus CH; Dailly R
    Sem Hop; 1974 Feb; 50(7):489-95. PubMed ID: 4367932
    [No Abstract]   [Full Text] [Related]  

  • 3. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
    Soyama K; Ono E
    Rinsho Byori; 1978 Dec; 26(12):1022-6. PubMed ID: 370427
    [No Abstract]   [Full Text] [Related]  

  • 4. Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy.
    Hug G; Schubert WK; Soukup S
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):160-83. PubMed ID: 4215475
    [No Abstract]   [Full Text] [Related]  

  • 5. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H; Goebel HH; Stefan H; Seidel D; Kohlschütter A
    J Clin Chem Clin Biochem; 1977 Dec; 15(12):705-8. PubMed ID: 342670
    [No Abstract]   [Full Text] [Related]  

  • 6. [The physiological segregation of glycogen. A precondition of the liver cell changes in glycogenosis type II (Pompe) (author's transl)].
    Pfeifer U
    Verh Dtsch Ges Pathol; 1971; 55():411-9. PubMed ID: 4130739
    [No Abstract]   [Full Text] [Related]  

  • 7. Enzyme therapy and prenatal diagnosis in glycogenosis type II.
    Hug G
    Am J Dis Child; 1974 Nov; 128(5):607-9. PubMed ID: 4278812
    [No Abstract]   [Full Text] [Related]  

  • 8. [Results of clinical, biochemical, light-microscopical and ultrastructural studies of childhood glycogenosis in two brothers and their sister (author's transl)].
    Ketelsen UP; Beckmann R; Nolte J; Menzel K
    Z Kinderheilkd; 1973 Dec; 116(1):23-41. PubMed ID: 4272442
    [No Abstract]   [Full Text] [Related]  

  • 9. Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetus.
    Benson PF; Blunt S; Brown SP; Nash FW; Tiller M
    Guys Hosp Rep; 1972; 121(2):137-46. PubMed ID: 4269382
    [No Abstract]   [Full Text] [Related]  

  • 10. Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease).
    Pokorny KS; Ritch R; Friedman AH; Desnick RJ
    Invest Ophthalmol Vis Sci; 1982 Jan; 22(1):25-31. PubMed ID: 6948796
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidase.
    de Barsy T; Jacquemin P; Van Hoof F; Hers HG
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):184-90. PubMed ID: 4611528
    [No Abstract]   [Full Text] [Related]  

  • 12. Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells.
    Hug G; Soukup S; Ryan M; Chuck G
    N Engl J Med; 1984 Apr; 310(16):1018-22. PubMed ID: 6369132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl)].
    Kölmel HW; Assmus H; Seiler D
    Arch Psychiatr Nervenkr (1970); 1974; 218(2):93-106. PubMed ID: 4522354
    [No Abstract]   [Full Text] [Related]  

  • 14. [Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)].
    Lück R; Platt D; Lange RH; Kunze K
    Z Kinderheilkd; 1975 Jul; 120(1):19-28. PubMed ID: 125955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal exclusion of Pompe disease by electron microscopy.
    Phupong V; Shotelersuk V
    Southeast Asian J Trop Med Public Health; 2006 Sep; 37(5):1021-4. PubMed ID: 17333749
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)].
    Harzer K; Zahn V; Stengel-Rutkowski S; Gley EO
    Dtsch Med Wochenschr; 1975 Apr; 100(17):951-3. PubMed ID: 1122864
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Histochemical and ultrastructural study of a case of type 3 glycogenosis].
    Chamlian A; Mariani R; Lafon J; Adechy-Benkoel L; Mounition L
    Ann Anat Pathol (Paris); 1971; 16(1):85-92. PubMed ID: 4327013
    [No Abstract]   [Full Text] [Related]  

  • 18. [Glycogenosis 3 - Pompe's disease - in a 1 1/2-month-old child].
    Papilova EI; Revenkova LA
    Pediatriia; 1975 May; (5):84-6. PubMed ID: 1056587
    [No Abstract]   [Full Text] [Related]  

  • 19. Fine structure of skeletal muscle in type-3 glycogenosis.
    Neustein HB
    Arch Pathol; 1969 Aug; 88(2):130-6. PubMed ID: 5256057
    [No Abstract]   [Full Text] [Related]  

  • 20. A micro-radiochemical assay for alpha-1,4-glucosidase and its use in the assessment of type II glycogenosis (Pompe's disease).
    Nelson PV; Carey WF; Pollard AC
    Clin Chim Acta; 1977 Jun; 77(3):337-42. PubMed ID: 17494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.