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 *

108 related articles for article (PubMed ID: 14226647)

  • 41. GENETICS AND ORTHOPAEDICS.
    NANCE WE; ELMORE SM; HILLMAN JW
    J Bone Joint Surg Am; 1965 Sep; 47():1260-71. PubMed ID: 14337787
    [No Abstract]   [Full Text] [Related]  

  • 42. [MOLECULAR DISEASES].
    SCATTINI CM
    Prensa Med Argent; 1964 Oct; 51():963-71. PubMed ID: 14231397
    [No Abstract]   [Full Text] [Related]  

  • 43. PHARMACOGENETICS--A NEW DISCIPLINE.
    NAHUM LH
    Conn Med; 1964 Dec; 28():857-8. PubMed ID: 14216218
    [No Abstract]   [Full Text] [Related]  

  • 44. Hepatic failure with acanthocytosis: association with hemolytic anemia and deficiency of erythrocyte glutathione peroxidase.
    Gharib H; Fairbanks VF; Bartholomew LG
    Mayo Clin Proc; 1969 Feb; 44(2):96-101. PubMed ID: 5764797
    [No Abstract]   [Full Text] [Related]  

  • 45. [GENETIC HETEROGENITY IN HUMAN ACATALASIA].
    HAMILTON HB; NEEL JV
    Jinrui Idengaku Zasshi; 1964 Mar; 9():46-56. PubMed ID: 14236257
    [No Abstract]   [Full Text] [Related]  

  • 46. FERROKINETICS IN PYRIDOXINE-RESPONSIVE ANAEMIA.
    ROATH S; BOURNE MS; ISRAUELS MC
    Acta Haematol; 1964 Jul; 32():1-8. PubMed ID: 14204454
    [No Abstract]   [Full Text] [Related]  

  • 47. PKU (PHENYLKETONURIA).
    NICKEY LN
    Southwest Med; 1964 Dec; 45():385-9. PubMed ID: 14232719
    [No Abstract]   [Full Text] [Related]  

  • 48. [HEGGLIN-MAY ANOMALY (POLYPHYLETIC MATURATION DISORDER)].
    HEGGLIN R; GROSS R; LOEHR GW
    Schweiz Med Wochenschr; 1964 Sep; 94():1357-64. PubMed ID: 14323323
    [No Abstract]   [Full Text] [Related]  

  • 49. [A family study on pyruvate kinase deficiency anemia].
    Helbig W; Jacobasch G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1969; 91(1):65-9. PubMed ID: 4180965
    [No Abstract]   [Full Text] [Related]  

  • 50. [Diet therapy of some inborn errors of metabolism].
    Perrone L
    Pediatria (Napoli); 1974 Sep; 82(2):260-97. PubMed ID: 4473102
    [No Abstract]   [Full Text] [Related]  

  • 51. [Acanthocytosis in a case of alcoholic cirrhosis with anemia. Acanthocytic transformation of transfused erythrocytes].
    Turpin F; Vaugier G; Bécart-Michel R; Binet JL
    Nouv Rev Fr Hematol; 1971; 11(5):791-8. PubMed ID: 4261194
    [No Abstract]   [Full Text] [Related]  

  • 52. Pathogenesis of celiac disease in adults. Compatibility of immunologic and enzyme-defect theories.
    Reed LS
    N Y State J Med; 1970 Aug; 70(16):2095-102. PubMed ID: 5269918
    [No Abstract]   [Full Text] [Related]  

  • 53. [Inborn errors of metabolism at the molecular level].
    Nakajima H
    Tanpakushitsu Kakusan Koso; 1968 Apr; 13(4):298-310. PubMed ID: 4881539
    [No Abstract]   [Full Text] [Related]  

  • 54. [Anderson's disease. Apropos of a new case].
    Polanco I; Mellado MJ; Lama R; Larrauri J; Zapata A; Redondo E; Vázquez C
    An Esp Pediatr; 1986 Mar; 24(3):185-8. PubMed ID: 3706925
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Secondary glutenogenic celiac disease with atypical course in a 10-month-old infant].
    Zareba J; Zieleźnik E
    Pol Tyg Lek; 1968 Oct; 23(42):1602-3. PubMed ID: 5702854
    [No Abstract]   [Full Text] [Related]  

  • 56. ENZYMES AND DRUG SENSITIVITY. THE GENETICS OF SERUM CHOLINESTERASE 'DEFICIENCY' IN RELATION TO SUXAMETHONIUM APNOEA.
    HARRIS H
    Proc R Soc Med; 1964 Jun; 57(6):503-6. PubMed ID: 14190871
    [No Abstract]   [Full Text] [Related]  

  • 57. Inborn errors of metabolism: some thoughts about their basic mechanisms.
    Howell RR
    Pediatrics; 1970 Jun; 45(6):901-5. PubMed ID: 4912255
    [No Abstract]   [Full Text] [Related]  

  • 58. Genetics and the physician.
    Delva PL
    N S Med Bull; 1965 Dec; 44(12):299-300. PubMed ID: 5215355
    [No Abstract]   [Full Text] [Related]  

  • 59. CLINICAL EVALUATION OF GENETIC DISEASES OF THE EYE.
    FALLS HF
    Trans Am Acad Ophthalmol Otolaryngol; 1965; 69():26-32. PubMed ID: 14259075
    [No Abstract]   [Full Text] [Related]  

  • 60. Disorders of lipid absorption.
    Muller DP
    Clin Gastroenterol; 1982 Jan; 11(1):119-40. PubMed ID: 7037235
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.