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 *

114 related articles for article (PubMed ID: 16942584)

  • 1. GM1-gangliosidosis type I.
    Pavlu J; Jackson M; Panoskaltsis N
    Br J Haematol; 2006 Nov; 135(4):422. PubMed ID: 16942584
    [No Abstract]   [Full Text] [Related]  

  • 2. Vacuolated lymphocytes and abnormal eosinophils in GM1 gangliosidosis, type 1.
    Chevalier C; Detry G
    Br J Haematol; 2012 Feb; 156(3):293. PubMed ID: 22053784
    [No Abstract]   [Full Text] [Related]  

  • 3. Neuroimaging findings in infantile GM1 gangliosidosis.
    Erol I; Alehan F; Pourbagher MA; Canan O; Vefa Yildirim S
    Eur J Paediatr Neurol; 2006; 10(5-6):245-8. PubMed ID: 17052929
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Non-neurological characteristics of Gm1 gangliosidosis type 1. A report of three cases within the same family].
    Bernal Ferrer A; Martí Barranco E; Tomás Vila M; Oltra Benavent M; Martinez Martinez J; Chabás A
    An Esp Pediatr; 1999 May; 50(5):513-6. PubMed ID: 10394196
    [No Abstract]   [Full Text] [Related]  

  • 5. Coincidental GM1 gangliosidosis in an infant with alpha-1-antitrypsin deficiency.
    Srinivasan R; Sudeendra S; Cosgrove M; Wagner B; Baker AJ; Portmann B
    J Pediatr Gastroenterol Nutr; 2008 Aug; 47(2):196-8. PubMed ID: 18664873
    [No Abstract]   [Full Text] [Related]  

  • 6. [GM1 syndrome, generalized infantile gangliosidosis. Presentation of two cases].
    Alvarez-Valiente H; Cuervo N; Dorado J; Menéndez C
    Rev Neurol; 1999 May 1-15; 28(9):926-8. PubMed ID: 10390761
    [No Abstract]   [Full Text] [Related]  

  • 7. Teaching neuroimages: T2 hypointense thalami in infantile GM1 gangliosidosis.
    Sharma S; Sankhyan N; Kabra M; Gulati S
    Neurology; 2010 Mar; 74(12):e47. PubMed ID: 20308674
    [No Abstract]   [Full Text] [Related]  

  • 8. [Clinical features of GM1 and GM2 gangliosidosis in own observation].
    Steczkowska M; Gergont A; Kroczka S; Nowak A
    Przegl Lek; 2008; 65(11):819-23. PubMed ID: 19205369
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Brain proton magnetic resonance spectroscopy and neuromuscular pathology in a patient with GM1 gangliosidosis.
    Brunetti-Pierri N; Bhattacharjee MB; Wang ZJ; Zili Chu ; Wenger DA; Potocki L; Hunter J; Scaglia F
    J Child Neurol; 2008 Jan; 23(1):73-8. PubMed ID: 18184943
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cerebrospinal fluid biomarkers showing neurodegeneration in dogs with GM1 gangliosidosis: possible use for assessment of a therapeutic regimen.
    Satoh H; Yamato O; Asano T; Yonemura M; Yamauchi T; Hasegawa D; Orima H; Arai T; Yamasaki M; Maede Y
    Brain Res; 2007 Feb; 1133(1):200-8. PubMed ID: 17196562
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Type 1 GM1 gangliosidosis with basal ganglia calcification: a case report.
    Chen CC; Chiu PC; Shieh KS
    Zhonghua Yi Xue Za Zhi (Taipei); 1999 Jan; 62(1):40-5. PubMed ID: 10063711
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of 14 novel GLB1 mutations, including five deletions, in 19 patients with GM1 gangliosidosis from South America.
    Santamaria R; Blanco M; Chabás A; Grinberg D; Vilageliu L
    Clin Genet; 2007 Mar; 71(3):273-9. PubMed ID: 17309651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extensive irregular Mongolian blue spots as a clue for GM1 gangliosidosis type 1.
    Bersani G; Guerriero C; Ricci F; Valentini P; Zampino G; Lazzareschi I; Antuzzi D; Rigante D
    J Dtsch Dermatol Ges; 2016 Mar; 14(3):301-2. PubMed ID: 26765271
    [No Abstract]   [Full Text] [Related]  

  • 14. Extensive and Progressing Congenital Dermal Melanocytosis Leading to Diagnosis of GM1 Gangliosidosis.
    Vedak P; Sells R; De Souza A; Hoang MP; Kroshinsky D
    Pediatr Dermatol; 2015; 32(6):e294-5. PubMed ID: 26337817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neuroimaging findings in late infantile GM1 gangliosidosis.
    Chen CY; Zimmerman RA; Lee CC; Chen FH; Yuh YS; Hsiao HS
    AJNR Am J Neuroradiol; 1998 Oct; 19(9):1628-30. PubMed ID: 9802482
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Gangliosidosis GM1 revelaed by Silverman syndrome].
    Ioos C; Lamer S; Picard A; Estournet-Mathiaut B; Pinard JM
    Arch Pediatr; 2000 Dec; 7(12):1353-4. PubMed ID: 11147074
    [No Abstract]   [Full Text] [Related]  

  • 17. Is there a relationship between extensive mongolian spots and inborn errors of metabolism?
    Silengo M; Battistoni G; Spada M
    Am J Med Genet; 1999 Nov; 87(3):276-7. PubMed ID: 10564887
    [No Abstract]   [Full Text] [Related]  

  • 18. Facial grimacing as a clue for the diagnosis of GM1 type 3 gangliosidosis.
    Maciel RO; Pedroso JL; Barsottini OG
    Arq Neuropsiquiatr; 2011; 69(2B):406-7. PubMed ID: 21625776
    [No Abstract]   [Full Text] [Related]  

  • 19. Comments on "type 3 GM1 gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl".
    Uyama E; Uchino M; Ando M
    J Neurol; 1996 Mar; 243(3):295-7. PubMed ID: 8936363
    [No Abstract]   [Full Text] [Related]  

  • 20. Mongolian spots are not always a benign sign.
    Hackbart BA; Arita JH; Pinho RS; Masruha MR; Vilanova LC
    J Pediatr; 2013 May; 162(5):1070. PubMed ID: 23374678
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.