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 *

163 related articles for article (PubMed ID: 14259271)

  • 1. A-BETA-LIPOPROTEINAEMIA.
    FORSYTH CC; LLOYD JK; FOSBROOKE AS
    Arch Dis Child; 1965 Feb; 40(209):47-51. PubMed ID: 14259271
    [No Abstract]   [Full Text] [Related]  

  • 2. A-BETA-LIPOPROTEINAEMIA WITH SPECIAL REFERENCE TO THE VISUAL DEFECT.
    WOLFF OH; LLOYD JK; TONKS EL
    Exp Eye Res; 1964 Dec; 3():439-42. PubMed ID: 14282999
    [No Abstract]   [Full Text] [Related]  

  • 3. CONGENITAL BETA-LIPOPROTEIN DEFICIENCY: AN HEREDITARY DISORDER INVOLVING A DEFECT IN THE ABSORPTION AND TRANSPORT OF LIPIDS.
    ISSELBACHER KJ; SCHEIG R; PLOTKIN GR; CAULFIELD JB
    Medicine (Baltimore); 1964 May; 43():347-61. PubMed ID: 14168744
    [No Abstract]   [Full Text] [Related]  

  • 4. A-BETA-LIPOPROTEINAEMIA (BASSEN-KORNZWEIG SYNDROME): REPORT OF A CASE.
    BECROFT DM; COSTELLO JM; SCOTT PJ
    Arch Dis Child; 1965 Feb; 40(209):40-6. PubMed ID: 14259270
    [No Abstract]   [Full Text] [Related]  

  • 5. RED-CELL AND PLASMA LIPIDS IN ACANTHOCYTOSIS.
    WAYS P; REED CF; HANAHAN DJ
    J Clin Invest; 1963 Aug; 42(8):1248-60. PubMed ID: 14060400
    [No Abstract]   [Full Text] [Related]  

  • 6. Bassen-Kornweig syndrome. Neuromuscular disorder resembling Friedreich's ataxia associated with retinitis pigmentosa, acanthocytosis, steatorrhea, and an abnormality of lipid metabolism.
    SCHWARTZ JF; ROWLAND LP; EDER HA; MARKS PM; OSSERMAN E; ANDERSON H; HIRSCHBERG E
    Trans Am Neurol Assoc; 1961; 86():49-53. PubMed ID: 13909703
    [No Abstract]   [Full Text] [Related]  

  • 7. [DISORDERS IN THE LIPID PATTERN IN A PATIENT WITH ACANTHOCYTOSIS AND IN SOME OF HIS FAMILY MEMBERS].
    HOOGHWINKEL GJ
    Ned Tijdschr Geneeskd; 1964 Sep; 108():1831-2. PubMed ID: 14226648
    [No Abstract]   [Full Text] [Related]  

  • 8. CELIAC SYNDROME, RETINAL DYSTROPHY, ACANTHOCYTOSIS, WITHOUT DEFECT OF BETA LIPOPROTEIN.
    TOLENTINO P; SPIRITO L; JANNUZZI C
    Ann Paediatr; 1964; 203():178-86. PubMed ID: 14212872
    [No Abstract]   [Full Text] [Related]  

  • 9. [Beta-lipoprotein deficiency syndromes. A-beta-lipoproteinemia and hypo-beta-lipoproteinemia].
    Gatti R; Vignola G; Macagno F; Nordio S
    Minerva Pediatr; 1969 Oct; 21(41):1887-92. PubMed ID: 5361987
    [No Abstract]   [Full Text] [Related]  

  • 10. Hereditary neurological disease with acanthocytosis. A new syndrome.
    Levine IM; Estes JW; Looney JM
    Arch Neurol; 1968 Oct; 19(4):403-9. PubMed ID: 5677189
    [No Abstract]   [Full Text] [Related]  

  • 11. Congenital absence of beta-lipoproteins.
    LAMY M; FREZAL J; POLONOVSKI J; DRUEZ G; REY J
    Pediatrics; 1963 Feb; 31():277-89. PubMed ID: 13928363
    [No Abstract]   [Full Text] [Related]  

  • 12. On having no beta-lipoprotein. A syndrome comprising a-beta-lipoproteinaemia, acanthocytosis, and steatorrhoea.
    SALT HB; WOLFF OH; LLOYD JK; FOSBROOKE AS; CAMERON AH; HUBBLE DV
    Lancet; 1960 Aug; 2(7146):325-9. PubMed ID: 13745738
    [No Abstract]   [Full Text] [Related]  

  • 13. A-beta-lipoproteinaemia and colour-blindness.
    Khachadurian AK; Freyha R; Shamma'a MM; Baghdassarian SA
    Arch Dis Child; 1971 Dec; 46(250):871-3. PubMed ID: 5316085
    [No Abstract]   [Full Text] [Related]  

  • 14. [OLIGOPHRENIA, CONGENITAL CATARACT, RETINITIS PIGMENTOSA, CEREBELLAR ATAXIA, NEUROGENIC AMYOTROPHIA. OBSERVATIONS ON 3 FAMILIAL CASES AND COMPARISON WITH THE MARINESCO-SJOGREN'S SYNDROME].
    CALVI LA
    Sist Nerv; 1963; 15():189-98. PubMed ID: 14073896
    [No Abstract]   [Full Text] [Related]  

  • 15. [ACANTHOCYTOSIS].
    STOECKER JP
    Ned Tijdschr Geneeskd; 1964 Sep; 108():1830-1. PubMed ID: 14226647
    [No Abstract]   [Full Text] [Related]  

  • 16. Hereditary chorioretinal degeneration and metabolic disturbances.
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):911-27. PubMed ID: 4190613
    [No Abstract]   [Full Text] [Related]  

  • 17. FAMILIAL NEPHROPATHY WITH RETINITIS PIGMENTOSA; A NEW OCULORENAL SYNDROME IN ADULTS.
    MEIER DA; HESS JW
    Am J Med; 1965 Jul; 39():58-69. PubMed ID: 14314238
    [No Abstract]   [Full Text] [Related]  

  • 18. [Anderson's disease].
    Polonovski C; Navarro J; Fontaine JL; de Gouyon F; Saudubray JM; Cathelineau L
    Ann Pediatr (Paris); 1970 May; 17(5):342-54. PubMed ID: 5421321
    [No Abstract]   [Full Text] [Related]  

  • 19. [CUTANEOUS AND MUCOUS LIPOPROTEINOSIS OR CUTANEOUS AND MUCOUS HYALINOSIS (URBACH-WIETHE DISEASE)].
    NOWAK T
    Helv Paediatr Acta; 1964 Jun; 19():69-77. PubMed ID: 14193811
    [No Abstract]   [Full Text] [Related]  

  • 20. [SYNDROME OF DEFECTIVE INTESTINAL ABSORPTION IN THE CHILD. (CELIAC SYNDROME)].
    MUNOZTURNBULL J
    Rev Colomb Pediatr Pueric; 1963 Jun; 21():133-48. PubMed ID: 14125658
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.