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 *

102 related articles for article (PubMed ID: 23622400)

  • 21. [Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)].
    Lubs H; Baumann H; Kluge G; Machill G
    Laryngol Rhinol Otol (Stuttg); 1974 Sep; 53(9):648-51. PubMed ID: 4419508
    [No Abstract]   [Full Text] [Related]  

  • 22. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
    Boisse J
    Presse Med (1893); 1968 Apr; 76(19):903-6. PubMed ID: 5645352
    [No Abstract]   [Full Text] [Related]  

  • 23. Non-ketotic hyperglycinemia in two sibs with mild psycho-neurological symptoms.
    Holmgren G; son Blomquist HK
    Neuropadiatrie; 1977 Feb; 8(1):67-72. PubMed ID: 576734
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Carnitine deficiency in inborn errors of metabolism].
    Sela BA; Lerman-Sagie T; Berkovitz M
    Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Glutaric aciduria type I. Clinical, biochemical and molecular findings in six patients in Venezuela].
    Mahfoud A; Domínguez CL; Rizzo C; García-Villoria J; Navarro-Sastre A; Ribes A
    Rev Neurol; 2007 May 16-31; 44(10):610-5. PubMed ID: 17523120
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multicentre age-related reference intervals for cerebrospinal fluid serine concentrations: implications for the diagnosis and follow-up of serine biosynthesis disorders.
    Moat S; Carling R; Nix A; Henderson M; Briddon A; Prunty H; Talbot R; Powell A; Wright K; Fuchs S; de Koning T
    Mol Genet Metab; 2010; 101(2-3):149-52. PubMed ID: 20692860
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Inherited hyperammonemia].
    Bik-Multanowski M
    Przegl Lek; 1998; 55(6):337-41. PubMed ID: 9857711
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant.
    Srisomsap' C; Wasant P; Svasti J; Chokchaichamnankit D; Liammongkolkul S
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():140-2. PubMed ID: 11400752
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Inherited abnormalities in amino acid metabolism].
    Farriaux JP
    Ann Anesthesiol Fr; 1977; 18(12):1053-62. PubMed ID: 24392
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Further results of studies on metabolic disorders in a population of severely retarded children (2)].
    Opałka S; Galewicz A; Pisarska E; Wegrzynowicz Z
    Psychiatr Neurol Med Psychol Beih; 1968; 8-9():126-9. PubMed ID: 5006367
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: an eight-year experience.
    Vatanavicharn N; Ratanarak P; Liammongkolkul S; Sathienkijkanchai A; Wasant P
    Clin Chim Acta; 2012 Jul; 413(13-14):1141-4. PubMed ID: 22465081
    [TBL] [Abstract][Full Text] [Related]  

  • 33. When do we need to perform a diagnostic lumbar puncture for neurometabolic diseases? Positive yield and retrospective analysis from a tertiary center.
    Haliloğlu G; Vezir E; Baydar L; Onol S; Sivri S; Coşkun T; Topçu M
    Turk J Pediatr; 2012; 54(1):52-8. PubMed ID: 22397043
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sibship with histidinemia and an unrelated encephalopathy. Clinical and biochemical studies.
    Brown ES; Waisman HA; Geison RL; Gerritsen T
    Helv Paediatr Acta; 1977 Nov; 32(4-5):401-11. PubMed ID: 617985
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Prenatal symptoms and diagnosis of inherited metabolic diseases].
    Brassier A; Ottolenghi C; Boddaert N; Sonigo P; Attié-Bitach T; Millischer-Bellaiche AE; Baujat G; Cormier-Daire V; Valayannopoulos V; Seta N; Piraud M; Chadefaux-Vekemans B; Vianey-Saban C; Froissart R; de Lonlay P
    Arch Pediatr; 2012 Sep; 19(9):959-69. PubMed ID: 22884749
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A new genetic defect of branched chain amino acid metabolism?
    Buneta D; Raić F; Lipovac K; Velikonja N
    Monogr Hum Genet; 1972; 6():130-40. PubMed ID: 4663885
    [No Abstract]   [Full Text] [Related]  

  • 37. [Cri-du-chat disease: plasma and urinary amino acids].
    Lejeune J; Rethoré MO; Peeters M; de Blois MC; Rabier D; Parvy P; Bardet J; Kamoun P
    Ann Genet; 1990; 33(1):16-20. PubMed ID: 2369068
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. A survey of inborn errors of amino acid metabolism and transport in man.
    Wellner D; Meister A
    Annu Rev Biochem; 1981; 50():911-68. PubMed ID: 6791581
    [No Abstract]   [Full Text] [Related]  

  • 40. Combination of BCAAs and glutamine enhances dermal collagen protein synthesis in protein-malnourished rats.
    Murakami H; Shimbo K; Takino Y; Kobayashi H
    Amino Acids; 2013 Mar; 44(3):969-76. PubMed ID: 23135226
    [TBL] [Abstract][Full Text] [Related]  

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