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 *

101 related articles for article (PubMed ID: 4041354)

  • 1. Malabsorption and polymyositis in a case of congenital methaemoglobinaemia.
    Packe GE; Kubik MM
    Br J Clin Pract; 1985 Jun; 39(6):250-1. PubMed ID: 4041354
    [No Abstract]   [Full Text] [Related]  

  • 2. Polymyositis as a cause of malabsorption. A case report.
    Transfeldt EE; Morley JE; Segal F; Klein A; Bill P; Fancourt M
    S Afr Med J; 1977 Feb; 51(6):176-8. PubMed ID: 841448
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis].
    Smith B; Pryds OA; Christensen E; Lund AM
    Ugeskr Laeger; 2008 Aug; 170(33):2460. PubMed ID: 18761834
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Small intestinal complications in progressive systemic sclerosis.
    Wilkinson MM
    Gastroenterol Nurs; 1992 Aug; 15(1):50-3. PubMed ID: 1525195
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Malabsorption polymyositis caused by narrowing of the celiac artery].
    Ledić P; Sepcić J; Milohanović S; Willheim K
    Neurologija; 1978; 26(1-4):149-51. PubMed ID: 754012
    [No Abstract]   [Full Text] [Related]  

  • 6. Why so blue? A case of neonatal cyanosis due to congenital methaemoglobinaemia (HbM Iwate).
    McGrath JS; Datir S; O'Brien F
    BMJ Case Rep; 2016 Nov; 2016():. PubMed ID: 27895078
    [No Abstract]   [Full Text] [Related]  

  • 7. [Congenital methemoglobinemia: a rare case of cyanosis in the newborn].
    Schwartz L; Franck P; Debruille C; Olivier JL; Vigneron C
    Ann Biol Clin (Paris); 2005; 63(3):314-6. PubMed ID: 15951263
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coexisting hereditary methaemoglobinaemia and heterozygous beta-thalassaemia.
    Kumar R; Tandon R; Badami KG
    Acta Paediatr Scand; 1989 Jan; 78(1):149-51. PubMed ID: 2919519
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Coexistence of congenital methemoglobinemia and cyanotic heart defect in a newborn infant].
    Maszkiewicz W; Manerowska D
    Wiad Lek; 1981 Feb; 34(4):313-6. PubMed ID: 7257405
    [No Abstract]   [Full Text] [Related]  

  • 10. A case with quadriparetic cerebral palsy and cyanosis: congenital methemoglobinemia.
    Gokalp S; Unuvar E; Oguz F; Kilic A; Sidal M
    Pediatr Neurol; 2005 Aug; 33(2):131-3. PubMed ID: 16087059
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Protein-losing enteropathy and malabsorption syndrome in a case of myxedema].
    Marano R; Pastore G; Strada C; Schiraldi O
    Arch Ital Mal Appar Dig; 1966; 33(2):115-26. PubMed ID: 5960382
    [No Abstract]   [Full Text] [Related]  

  • 12. [Congenital familial methemoglobinemia. A brother and a sister, both with encephalopathy].
    Knudsen L
    Ugeskr Laeger; 1974 May; 136(22):1200-2. PubMed ID: 4840774
    [No Abstract]   [Full Text] [Related]  

  • 13. Methaemoglobinaemia--a rare cause of myocardial ischaemia.
    Gupta AK; Chaudhary HR; Jain UB
    J Assoc Physicians India; 1990 Dec; 38(12):954-5. PubMed ID: 2096144
    [No Abstract]   [Full Text] [Related]  

  • 14. Polymyositis and myelodysplastic syndrome.
    Asman A; Ehrenfeld M; Sadeh M; Feldman S; Samra Y
    J Rheumatol; 1991 Aug; 18(8):1272-4. PubMed ID: 1941845
    [No Abstract]   [Full Text] [Related]  

  • 15. [Congenital methemoglobinemia with central nervous system damage caused by generalized deficiency of NADH-dependent methemoglobin reductase in a 2-year-old Polish girl].
    Holtorp-Tyszkiewiczowa J; Jabłońska-Skwiecińska E; Szmidt-Sidor B; Wierzbicka D
    Pediatr Pol; 1984 Oct; 59(10):865-70. PubMed ID: 6533561
    [No Abstract]   [Full Text] [Related]  

  • 16. [Respiratory insufficiency caused by dapsone-induced methemoglobinemia].
    Ipsen SE; Hansen VE
    Ugeskr Laeger; 2001 Jan; 163(1):39-40. PubMed ID: 11586671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Life-threatening diarrhea in the neonatal period. A case of congenital glucose-galactose malabsorption].
    Bangstad HJ
    Tidsskr Nor Laegeforen; 1982 Nov; 102(33):1757-8. PubMed ID: 7167947
    [No Abstract]   [Full Text] [Related]  

  • 18. NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I.
    Percy MJ; Aslan D
    J Clin Pathol; 2008 Oct; 61(10):1122-3. PubMed ID: 18820099
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A stiff man with malabsorption.
    Rae SA; Rose PE; Powell-Jackson P; Goodwill CJ; Fernandes L; Berry H; Scott JT
    J R Soc Med; 1988 Feb; 81(2):115-7. PubMed ID: 3346854
    [No Abstract]   [Full Text] [Related]  

  • 20. [Congenital methemoglobinemia].
    Arrigoni GA; Sanson A; Ronzon N; Cantarini G
    Folia Hered Pathol (Milano); 1968 Jan; 17(1):1-16. PubMed ID: 5732816
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.