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 *

122 related articles for article (PubMed ID: 4834781)

  • 1. Emotional deprivation. Report of a case with features of leprechaunism.
    Hopwood NJ; Powell GF
    Am J Dis Child; 1974 Jun; 127(6):892-4. PubMed ID: 4834781
    [No Abstract]   [Full Text] [Related]  

  • 2. Leprechaunism (Donohue syndrome). A case with growth hormone deficiency.
    Gillerot Y; Buez A; Hustin J
    Acta Paediatr Belg; 1979; 32(4):279-80. PubMed ID: 546030
    [No Abstract]   [Full Text] [Related]  

  • 3. [A case of leprechaunism].
    La Selve P; Louis JJ; Feit JP; Guibaud P; Larbre F
    Pediatrie; 1982 Dec; 37(8):607-13. PubMed ID: 6763675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of leprechaunism and an analysis of some clinical manifestations of this syndrome.
    Tsujino G
    Z Kinderheilkd; 1975; 118(4):347-60. PubMed ID: 1130123
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leprechaunism (Donohue's syndrome): a case report.
    Summitt RL; Favara BE
    J Pediatr; 1969 Apr; 74(4):601-10. PubMed ID: 4886189
    [No Abstract]   [Full Text] [Related]  

  • 6. [Leprechaunism (Donohue syndrome)].
    Fujieda K
    Nihon Rinsho; 2006 Sep; Suppl 3():94-9. PubMed ID: 17022508
    [No Abstract]   [Full Text] [Related]  

  • 7. Intrauterine growth retardation, jaundice, and hypoglycemia in a neonate.
    Ordway NK; Stout LC
    J Pediatr; 1973 Nov; 83(5):867-74. PubMed ID: 4742585
    [No Abstract]   [Full Text] [Related]  

  • 8. [The Silver-Russel syndrome].
    Sarotti M; Zilocchi C; Bianchi P; Faraci C; Marenzi C; Martinelli D; Escobar R
    Pediatr Med Chir; 1992; 14(2):227-30. PubMed ID: 1508761
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Donohue's syndrome (leprechaunism) in a female infant.
    Poradovska W; Jaworska M; Hanc I
    Acta Chir Plast; 1972; 14(1):4-12. PubMed ID: 4112399
    [No Abstract]   [Full Text] [Related]  

  • 10. [Leprechaunism (Donohue's syndrome)].
    Poradowska W; Jaworska M; Hanc I
    Pediatr Pol; 1972; 47(3):345-8. PubMed ID: 5019699
    [No Abstract]   [Full Text] [Related]  

  • 11. [Leprechaunism].
    Koya G
    Nihon Rinsho; 1977; 35 Suppl 1():1168-9. PubMed ID: 612775
    [No Abstract]   [Full Text] [Related]  

  • 12. [Leprechaunism. New case and review].
    Canlorbe P; Allaire Y; Lelong M
    Ann Pediatr (Paris); 1968 Apr; 15(4):1074-83. PubMed ID: 5743018
    [No Abstract]   [Full Text] [Related]  

  • 13. [Case of leprechaunism in a girl].
    Badalian LO; Petrukhin AS; Filina NP
    Pediatriia; 1980 Dec; (12):24-7. PubMed ID: 7220166
    [No Abstract]   [Full Text] [Related]  

  • 14. Leprechaunism. Case report in a black African child.
    Hartdegen RG; Dogliotti M; Rabinowitz L; Bartlett RG
    Br J Dermatol; 1975 Nov; 93(5):587-91. PubMed ID: 1203183
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leprechaunism: report of two cases and review.
    Ioan D; Dumitriu L; Belengeanu V; Bistriceanu M; Maximilian C
    Endocrinologie; 1988; 26(3):205-9. PubMed ID: 3062757
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leprechaunism. A report of two new cases.
    Der Kaloustian VM; Kronfol NM; Takla R; Habash A; Khazin A; Najjar SS
    Am J Dis Child; 1971 Nov; 122(5):442-5. PubMed ID: 5129536
    [No Abstract]   [Full Text] [Related]  

  • 17. [Leprechaunism or Donohue's syndrome. Clinical and chromosome study of a male patient].
    Giovannucci ML; Calabri G; Carattoli MG
    Haematologica; 1969; 54(12):875-89. PubMed ID: 4993254
    [No Abstract]   [Full Text] [Related]  

  • 18. A case of chromosome abnormality (46, XX, Gq+) with congenital heart disease and leprechaunism.
    Iwaski H; Abe M; Nawate G; Kato H
    Jinrui Idengaku Zasshi; 1974 Jun; 19(1):82-3. PubMed ID: 4476865
    [No Abstract]   [Full Text] [Related]  

  • 19. Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent de novo mutation in the POLD1 gene.
    Sasaki H; Yanagi K; Ugi S; Kobayashi K; Ohkubo K; Tajiri Y; Maegawa H; Kashiwagi A; Kaname T
    Endocr J; 2018 Feb; 65(2):227-238. PubMed ID: 29199204
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Cockayne's syndrome].
    Brezina Z; Dockalova M
    Kinderarztl Prax; 1976 Jun; 44(6):259-62. PubMed ID: 940287
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.