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Journal Abstract Search

481 related items for PubMed ID: 4254502

  • 1. [Hereditary mucopolysaccharidoses].
    Spranger J.
    Med Klin; 1971 Aug 13; 66(23):1105-12. PubMed ID: 4254502
    [No Abstract] [Full Text] [Related]

  • 2. [Mucopolysaccharidoses].
    Blehová B, Pazoutová N, Brychnác V.
    Cas Lek Cesk; 1972 Aug 13; 111(8):186-9. PubMed ID: 4258700
    [No Abstract] [Full Text] [Related]

  • 3. [Mucopolysaccharidoses].
    Lenoch F.
    Fysiatr Revmatol Vestn; 1970 Oct 13; 48(5):197-206. PubMed ID: 4248391
    [No Abstract] [Full Text] [Related]

  • 4. [Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses].
    Passarge E, Wendel U, Wöhler W, Rüdiger HW.
    Dtsch Med Wochenschr; 1974 Jan 25; 99(4):144 passim. PubMed ID: 4274189
    [No Abstract] [Full Text] [Related]

  • 5. [Diagnosis of hereditary mucopolysaccharidoses].
    Onisawa J, Ri N, Nakamura R, Mizuno T, Suzuki Y.
    Nihon Hifuka Gakkai Zasshi; 1972 Sep 25; 82(9):667-73. PubMed ID: 4265653
    [No Abstract] [Full Text] [Related]

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  • 8. [Mucopolysaccharidosis--synthesis and prospects].
    Bulgarelli R, Romano C.
    Minerva Pediatr; 1972 Oct 13; 24(35):1703-5. PubMed ID: 4264768
    [No Abstract] [Full Text] [Related]

  • 9. [Clinical variants of hereditary mucopolysaccharidosis].
    Geller LI.
    Klin Med (Mosk); 1970 Jul 13; 48(7):16-9. PubMed ID: 4250220
    [No Abstract] [Full Text] [Related]

  • 10. [Recent data on mucopolysaccharidoses].
    Spranger J.
    Monatsschr Kinderheilkd (1902); 1973 May 13; 121(5):181-3. PubMed ID: 4268292
    [No Abstract] [Full Text] [Related]

  • 11. The nosology of the mucopolysaccharidoses.
    McKusick VA.
    Am J Med; 1969 Nov 13; 47(5):730-47. PubMed ID: 4242813
    [No Abstract] [Full Text] [Related]

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  • 14. [Mucopolysaccharidoses. IV. Morphological contribution to the knowledge of mucopolysaccharidosis].
    Magrini U, Scappaticci S.
    Minerva Pediatr; 1972 Oct 06; 24(34):1609-28. PubMed ID: 4264143
    [No Abstract] [Full Text] [Related]

  • 15. A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI).
    Baron RW, Neufeld EF.
    J Pediatr; 1972 Jan 06; 80(1):114-6. PubMed ID: 4259536
    [No Abstract] [Full Text] [Related]

  • 16. The detection of carriers and the problem of heterogeneity in genetic counseling.
    Porter IH.
    Birth Defects Orig Artic Ser; 1970 May 06; 6(1):23-5. PubMed ID: 4257329
    [No Abstract] [Full Text] [Related]

  • 17. [The mucopolysaccharidoses in childhood. Clinical study].
    De Angelis P.
    Pediatria (Napoli); 1967 May 06; 75(4):561-82. PubMed ID: 4231289
    [No Abstract] [Full Text] [Related]

  • 18. [Genetically determined mucopolysaccharidoses in children].
    Badalian LO, Gusev EI, Guseva MR.
    Pediatriia; 1971 Mar 06; 50(3):58-62. PubMed ID: 4254530
    [No Abstract] [Full Text] [Related]

  • 19. Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy.
    McKusick VA, Howell RR, Hussels IE, Neufeld EF, Stevenson RE.
    Trans Assoc Am Physicians; 1972 Mar 06; 85():151-71. PubMed ID: 4267098
    [No Abstract] [Full Text] [Related]

  • 20. [Heritable disorders of the connective tissue].
    Friman C, Näntö V.
    Duodecim; 1969 Mar 06; 85(18):1155-69. PubMed ID: 4244410
    [No Abstract] [Full Text] [Related]

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