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 *

63 related articles for article (PubMed ID: 705137)

  • 1. [Cerebellar atrophy in a patient with dextrocardia, eosinophilia, congenital strabismus and familial chromatographic alterations of serum amino acids].
    Ionescu M; Login S; Iordache C
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1978; 23(2):123-30. PubMed ID: 705137
    [No Abstract]   [Full Text] [Related]  

  • 2. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G; Farriaux JP; Dautrevaux M
    Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477
    [No Abstract]   [Full Text] [Related]  

  • 3. Hydroxyprolinemia: an apparently harmless familial metabolic disorder.
    Pelkonen R; Kivirikko KI
    N Engl J Med; 1970 Aug; 283(9):451-6. PubMed ID: 4393577
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial cerebellar atrophy.
    Sullivan JA; McConnell JR; Woody RC
    J Ark Med Soc; 1985 Mar; 81(10):497-9. PubMed ID: 3157669
    [No Abstract]   [Full Text] [Related]  

  • 5. [Are there various forms of gyrate atrophy of the choroid and retina? (choroidal and retinal gyrate atrophy with and without ornithinemia)].
    Jaeger W; von Kettler J; Hilsdorf C; Lutz P
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1978; (75):655-63. PubMed ID: 743182
    [No Abstract]   [Full Text] [Related]  

  • 6. [Relation between metabolic amino acid defect and familial occurring epilepsy].
    Bárdosová G; Králik M; Lazorová A; Mäsiar P; Adam J
    Psychiatr Neurol Med Psychol Beih; 1970; 13-14():182-90. PubMed ID: 5006283
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hypersarcosinemia with sarcosinuria. Study of a new case].
    Willems C; Heusden A; Hainaut A; Chapelle P
    J Genet Hum; 1971 Mar; 19(1):101-18. PubMed ID: 5158355
    [No Abstract]   [Full Text] [Related]  

  • 8. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
    Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
    Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972
    [No Abstract]   [Full Text] [Related]  

  • 9. [Results of screening for aminoacidopathies in pregnant women].
    Hyánek J; Trnka V; Homolka J; Vácha V; Srácek J; Cervenka J; Dolezal A; Seemanová E; Kapras J; Malá M; Wünschová N; Holub J; Hoza J; Losan F; Nevsímalová S; Kubík M; Viletová H; Ronová R; Kunová V; Matousová M
    Cesk Pediatr; 1977 Aug; 32(8):460-3. PubMed ID: 597929
    [No Abstract]   [Full Text] [Related]  

  • 10. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J; Guardiola Vicente JM; Botella García J
    Rev Clin Esp; 1970 Jul; 118(2):141-50. PubMed ID: 5486371
    [No Abstract]   [Full Text] [Related]  

  • 11. Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy.
    Kish SJ; Robitaille Y; el-Awar M; Gilbert J; Deck J; Chang LJ; Schut L
    Ann Neurol; 1991 Dec; 30(6):780-4. PubMed ID: 1686387
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial pancreatitis associated with hyperglycinuria.
    Bergström K; Hellström K; Kallner M; Lundh G
    Scand J Gastroenterol; 1973; 8(3):217-23. PubMed ID: 4724921
    [No Abstract]   [Full Text] [Related]  

  • 13. [Lethal familial neonatal ketotic hyperammonemia].
    Pauli A; Huguet J; Rollet M; Cousin J; Farriaux JP; Fournier A; Navarro J; Cathelineau L; Aymard P; Saudubray JM; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):699-712. PubMed ID: 4644460
    [No Abstract]   [Full Text] [Related]  

  • 14. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA; Ismail Z; Embong KH; Mohamad SA
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Personal experience with chromatographic methods of demonstrating aminated substances (amino acids and amines)].
    Berio A
    Minerva Pediatr; 1968 Mar; 20(10):536-45. PubMed ID: 5739013
    [No Abstract]   [Full Text] [Related]  

  • 16. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F; Pavone L; Antener I
    Pediatrics; 1971 Aug; 48(2):225-31. PubMed ID: 5560617
    [No Abstract]   [Full Text] [Related]  

  • 17. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial essential hyperprolinemia].
    Hainaut H; Hariga J; Willems C; Heusden A; Chapelle P
    Presse Med (1893); 1971 Apr; 79(21):945-8. PubMed ID: 5580522
    [No Abstract]   [Full Text] [Related]  

  • 19. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract]   [Full Text] [Related]  

  • 20. [Personal results in screening amino acid diseases by means of the method of Scriver et al].
    Di Stefano A; Berio A; Viglione M; Liotta A; Piovano B; Bellati R
    Minerva Pediatr; 1970 Mar; 22(10):461-70. PubMed ID: 5444384
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.