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 *

116 related articles for article (PubMed ID: 3532855)

  • 1. Julius Caesar and the Julian emperors. A family cluster with Hartnup disease?
    Dirckx JH
    Am J Dermatopathol; 1986 Aug; 8(4):351-7. PubMed ID: 3532855
    [No Abstract]   [Full Text] [Related]  

  • 2. Searching for neurological diseases in the Julio-Claudian dynasty of the Roman Empire.
    Camargo CHF; Teive HAG
    Arq Neuropsiquiatr; 2018 Jan; 76(1):53-57. PubMed ID: 29364395
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hartnup disorder in a New England family.
    Pomeroy J; Efron ML; Dayman J; Hoefnagel D
    N Engl J Med; 1968 May; 278(22):1214-6. PubMed ID: 5647741
    [No Abstract]   [Full Text] [Related]  

  • 4. Asthma among the famous. Augustus Caesar (63 B.C.-A.D. 14) first emperor of Rome.
    King JR; Cohen SG
    Allergy Asthma Proc; 2001; 22(2):101-9. PubMed ID: 11332291
    [No Abstract]   [Full Text] [Related]  

  • 5. Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.
    Shih VE; Coulombe JT; Wadman SK; Duran M; Waelkens JJ
    Clin Genet; 1984 Sep; 26(3):216-20. PubMed ID: 6478642
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hartnup disease.
    Oyanagi K; Takagi M; Kitabatake M; Nakao T
    Tohoku J Exp Med; 1967 Apr; 91(4):383-95. PubMed ID: 4228120
    [No Abstract]   [Full Text] [Related]  

  • 7. Julius Caesar's Epilepsy: Was It Caused by A Brain Arteriovenous Malformation?
    Montemurro N; Benet A; Lawton MT
    World Neurosurg; 2015 Dec; 84(6):1985-7. PubMed ID: 26118720
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Has the diagnosis of a stroke been overlooked in the symptoms of Julius Caesar?
    Galassi FM; Ashrafian H
    Neurol Sci; 2015 Aug; 36(8):1521-2. PubMed ID: 25820216
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
    Kleta R; Romeo E; Ristic Z; Ohura T; Stuart C; Arcos-Burgos M; Dave MH; Wagner CA; Camargo SR; Inoue S; Matsuura N; Helip-Wooley A; Bockenhauer D; Warth R; Bernardini I; Visser G; Eggermann T; Lee P; Chairoungdua A; Jutabha P; Babu E; Nilwarangkoon S; Anzai N; Kanai Y; Verrey F; Gahl WA; Koizumi A
    Nat Genet; 2004 Sep; 36(9):999-1002. PubMed ID: 15286787
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Child poverty in ancient Rome: the 'Alimenta Italiae' of the "Good Emperors.".
    Aterman K
    Wurzbg Medizinhist Mitt; 1997; 16():151-72. PubMed ID: 11619720
    [No Abstract]   [Full Text] [Related]  

  • 11. Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder.
    Nozaki J; Dakeishi M; Ohura T; Inoue K; Manabe M; Wada Y; Koizumi A
    Biochem Biophys Res Commun; 2001 Jun; 284(2):255-60. PubMed ID: 11394870
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Julius Caesar (100-44 BC)--did he have a brain tumour?
    Retief FP; Cilliers JF
    S Afr Med J; 2010 Jan; 100(1):26-8. PubMed ID: 20429483
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hartnup disease (apropos of 2 initial cases in African Negroes)].
    Strobel M; Fall M; Kuakuvi N; N'Diaye B; Sanokho A; Marchand JP
    Bull Soc Med Afr Noire Lang Fr; 1978; 23(2):118-23. PubMed ID: 668033
    [No Abstract]   [Full Text] [Related]  

  • 14. The Caesars - Julius, Augustus and Claudius, a medical evaluation.
    Gluckman LK
    Scalpel Tongs; 1998; 42():76-80. PubMed ID: 11620466
    [No Abstract]   [Full Text] [Related]  

  • 15. Hartnup disorder: polymorphisms identified in the neutral amino acid transporter SLC1A5.
    Potter SJ; Lu A; Wilcken B; Green K; Rasko JE
    J Inherit Metab Dis; 2002 Oct; 25(6):437-48. PubMed ID: 12555937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Natural history of Hartnup disease.
    Wilcken B; Yu JS; Brown DA
    Arch Dis Child; 1977 Jan; 52(1):38-40. PubMed ID: 836052
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.
    Seow HF; Bröer S; Bröer A; Bailey CG; Potter SJ; Cavanaugh JA; Rasko JE
    Nat Genet; 2004 Sep; 36(9):1003-7. PubMed ID: 15286788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Letter: Permanent indicanuria. Heterozygote form of Hartnup's disease?].
    Thomas J; Hernandorena X; Aubry P; Le Bras R; Zimmer C
    Nouv Presse Med; 1975 Mar; 4(9):672. PubMed ID: 1129136
    [No Abstract]   [Full Text] [Related]  

  • 19. [Hartnup disease. Observations on a further case].
    Guzzetta F; Mazzaglia E
    Minerva Pediatr; 1970 Mar; 22(10):480-6. PubMed ID: 5444386
    [No Abstract]   [Full Text] [Related]  

  • 20. Hartnup disease. A report on two siblings.
    Somasundaram O; Papakumari M
    Indian Pediatr; 1973 Jul; 10(7):455-7. PubMed ID: 4761306
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.