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 *

132 related articles for article (PubMed ID: 879119)

  • 21. [Exomphalos-macroglossia-gigantism syndrome (Wiedmann-Beckwith syndrome)].
    Hanasono H
    Nihon Shonika Gakkai Zasshi; 1971 Jun; 75(6):435-9. PubMed ID: 5104629
    [No Abstract]   [Full Text] [Related]  

  • 22. [Exaggerated somatomedin activity in the Beckwith-Wiedemann syndrome (author's transl)].
    Schabel F; Frisch H
    Padiatr Padol; 1979; 14(3):249-57. PubMed ID: 471523
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism).
    Irving IM
    Prog Pediatr Surg; 1970; 1():1-61. PubMed ID: 4942287
    [No Abstract]   [Full Text] [Related]  

  • 24. [Wiedemann-Beckwith syndrome. Study of an oligosymptomatic form].
    Lemke J; Meinecke P; Frank HD
    Monatsschr Kinderheilkd; 1986 Aug; 134(8):554-7. PubMed ID: 3773923
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The Wiedemann-Beckwith syndrome].
    Bene M
    Rev Pediatr Obstet Ginecol Pediatr; 1978; 27(1):75-81. PubMed ID: 418483
    [No Abstract]   [Full Text] [Related]  

  • 26. Clinical profile in three patients with Beckwith-Wiedemann syndrome.
    Verma IC; Goswami HL; Rohtagi M; Singh M; Upadhyaya P
    Indian Pediatr; 1975 Jun; 12(6):509-13. PubMed ID: 1184150
    [No Abstract]   [Full Text] [Related]  

  • 27. Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome.
    Lubinsky M; Herrmann J; Kosseff AL; Opitz JM
    Lancet; 1974 May; 1(7863):932. PubMed ID: 4133452
    [No Abstract]   [Full Text] [Related]  

  • 28. Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential.
    Sotelo-Avila C; Gonzalez-Crussi F; Fowler JW
    J Pediatr; 1980 Jan; 96(1):47-50. PubMed ID: 7350313
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [On the "Kerben-Ohr" (inherited slit-like indentations of ear-lobes) in the Exomphalos-Macroglossia-Gigantism Syndrome, on auricular fistulae and on the presence of analogous findings in other syndromes and in normal individuals (author's transl)].
    Wiedemann HR
    Z Kinderheilkd; 1973 Aug; 115(2):95-110. PubMed ID: 4744211
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hemihypertrophy with wiedemann-Beckwith-syndrome (author's transl)].
    Schenck RD
    Z Orthop Ihre Grenzgeb; 1976 Jun; 114(3):354-60. PubMed ID: 941479
    [No Abstract]   [Full Text] [Related]  

  • 31. [Exomphalos-macroglossia-gigantism syndrome from the surgical viewpoint (EMG-syndrome)].
    Reuter G
    Zentralbl Chir; 1974 May; 99(21):668-72. PubMed ID: 4848705
    [No Abstract]   [Full Text] [Related]  

  • 32. [The EMG-syndrome: exomphalos, macroglossia, gigantism and disturbed carbohydrate metabolism].
    Wiedemann HR
    Z Kinderheilkd; 1969; 106(3):171-85. PubMed ID: 5797233
    [No Abstract]   [Full Text] [Related]  

  • 33. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.
    Berry AC; Belton EM; Chantler C
    J Med Genet; 1980 Apr; 17(2):136-8. PubMed ID: 7189783
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Clinical case of the Wiedemann-Beckwith syndrome].
    Buttitta P; Pasta G
    Minerva Pediatr; 1977 Apr; 29(12):855-8. PubMed ID: 875961
    [No Abstract]   [Full Text] [Related]  

  • 35. Further studies of the hypoglycemia in children with the exomphalos--macroglossia--gigantism syndrome.
    Grunt JA; Enriquez AR
    Yale J Biol Med; 1972 Feb; 45(1):15-21. PubMed ID: 5015569
    [No Abstract]   [Full Text] [Related]  

  • 36. Macroglossia in the Beckwith-Wiedemann syndrome.
    Grace JB; Heroman WM; Kornblut AD
    Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol; 1977; 84(1):116-9. PubMed ID: 855081
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Wiedemann-Beckwith syndrome. Description of a clinical case with macroglossia, umbilical hernia, hepatonephromegaly, relative microcephaly, macrosomy, and transient hypoglycemia].
    Lendvai D; Cardi E; Ballati G; Rezza E
    Pediatria (Napoli); 1968 Oct; 76(5):738-47. PubMed ID: 5739619
    [No Abstract]   [Full Text] [Related]  

  • 38. [Wiedemann-Beckwith syndrome (omphalocele-macroglossia-gigantism)].
    Hooft C; Boedts F; Van Acker K
    Ann Pediatr (Paris); 1969 Jan; 16(1):49-56. PubMed ID: 5791875
    [No Abstract]   [Full Text] [Related]  

  • 39. Hypertension and medullary sponge kidneys in an adolescent with Beckwith-Wiedemann syndrome.
    Virdis R; Drayer JI; Montoliu J; Levine LS; Laragh JH
    J Pediatr; 1977 Nov; 91(5):761-3. PubMed ID: 909016
    [No Abstract]   [Full Text] [Related]  

  • 40. [Exomphalos-macroglossia-gigantism, EMG syndrome].
    Velemínský M; Ríha F; Nováková E; Zizka K
    Cesk Pediatr; 1979 Jul; 34(7):421-2. PubMed ID: 487479
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.