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 *

103 related articles for article (PubMed ID: 8497333)

  • 1. [Type D Sanfilippo disease in an 8-year-old boy; a rare cause of mental retardation].
    del Canho H; van den Bergh FA; Duran M; Hennekam RC; Gröniger AM; Poorthuis BJ
    Ned Tijdschr Geneeskd; 1993 May; 137(19):969-72. PubMed ID: 8497333
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sanfilippo's syndrome type C--the first known case in South Africa.
    Petersen EM
    S Afr Med J; 1986 Jan; 69(1):63-8. PubMed ID: 3079922
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chronic subdural hematoma associated with mucopolysaccharidosis type III B (Sanfilippo's syndrome B).
    Kawasaki T; Kitagawa M; Suzuki K; Wataya T
    Childs Nerv Syst; 2016 May; 32(5):769-70. PubMed ID: 26951158
    [No Abstract]   [Full Text] [Related]  

  • 4. [Hyperactivity and behavioral disorders in Sanfilippo A (mucopolysaccharidosis type IIIA)--case report and review of the literature].
    Wolańczyk T; Banaszkiewicz A; Mierzewska H; Czartoryska B; Zdziennicka E
    Psychiatr Pol; 2000; 34(5):831-7. PubMed ID: 11202024
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Mucopolysaccharidosis III (Sanfilippo's syndrome): phenotypic characterization].
    Mendes FT; Ciorlia VR; Lamego C; de Almeida SP; de Ulhoa-Cintra AB
    Rev Hosp Clin Fac Med Sao Paulo; 1976; 31(6):478-83. PubMed ID: 827800
    [No Abstract]   [Full Text] [Related]  

  • 6. [Chronic plumbism in siblings with Sanfilippo's mucopolysaccharidosis].
    Hager-Malecka B; Sroczyńska M; Sychlowy A; Sońta-Jakimczyk D; Dziuba P; Król J
    Pediatr Pol; 1977 Jun; 52(6):659-63. PubMed ID: 406592
    [No Abstract]   [Full Text] [Related]  

  • 7. Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: report of one case.
    Lin SC; Hu FR; Hou JW; Yao YT; Wang TR; Hung PT
    Acta Paediatr Taiwan; 1999; 40(1):46-9. PubMed ID: 10910587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Sanfilippo's disease--accompanying findings in maxillofacial surgery as an aid to differential diagnosis of type III mucopolysaccharidosis].
    Radtke J
    Dtsch Z Mund Kiefer Gesichtschir; 1988; 12(4):289-92. PubMed ID: 3149221
    [No Abstract]   [Full Text] [Related]  

  • 9. Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type A.
    Kara S; Sherr EH; Barkovich AJ
    Pediatr Neurol; 2008 May; 38(5):363-6. PubMed ID: 18410855
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A comparative clinical, radiologic, biochemical and genetic study of Sanfilippo's disease, type A and B. Six case reports].
    Farriaux JP; Dhondt JL; Blanckaert D; Fontaine G
    Helv Paediatr Acta; 1974 Oct; 29(4):349-70. PubMed ID: 4214802
    [No Abstract]   [Full Text] [Related]  

  • 11. Morphological and biochemical findings in a case of mucopolysaccharidosis type III A (Sanfilippo's disease type A).
    Witting C; Müller KM; Kresse H; Figura KV; Marx H
    Beitr Pathol; 1975; 154(3):324-38. PubMed ID: 805586
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ruling out fetal Sanfilippo's syndrome (mucopolysaccharidosis IIIA) in the first trimester of pregnancy].
    Bolodár A; Török O; Szabó M; Váradi V; Papp Z
    Orv Hetil; 1989 Jan; 130(5):233-4. PubMed ID: 2492654
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autofluorescence emission spectra of neuronal lipopigment in mucopolysaccharidosis (Sanfilippo's syndrome).
    Dowson JH; Wilton-Cox H; Oldfors A; Sourander P
    Acta Neuropathol; 1989; 77(4):426-9. PubMed ID: 2496579
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Proceedings: The Sanfilippo syndrome.
    Staalman CR
    Radiol Clin (Basel); 1977; 46(2):156. PubMed ID: 402678
    [No Abstract]   [Full Text] [Related]  

  • 15. A variant of Fine-Lubinsky syndrome: a Japanese boy with profound deafness, cataracts, mental retardation, and brachycephaly without craniosynostosis.
    Nakane T; Mizobe N; Hayashibe H; Nakazawa S
    Clin Dysmorphol; 2002 Jul; 11(3):195-8. PubMed ID: 12072800
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Type III mucopolysaccharidosis (Sanfilippo's disease)].
    Vranjeĕvić D; Jović N; Stepanović R
    Srp Arh Celok Lek; 1988 Mar; 116(3):247-56. PubMed ID: 3137665
    [No Abstract]   [Full Text] [Related]  

  • 17. [Importance of radiographic diagnosis of the skull in mucopolysaccharidosis].
    Romano C; Pellizza A; Cordone G; Gargani GF; Grossi Bianchi ML
    Minerva Pediatr; 1975 Mar; 27(9):529-36. PubMed ID: 806779
    [No Abstract]   [Full Text] [Related]  

  • 18. [1st Italian family affected by type A Sanfilippo's disease].
    Carlomagno S; Militerni R; Pascotto A; Guazzi GC
    Acta Neurol (Napoli); 1977; 32(1):97-107. PubMed ID: 404848
    [No Abstract]   [Full Text] [Related]  

  • 19. Hemiatrophy of the spinal cord in a patient with mucopolysaccharidosis type IIIB.
    Samia P; Wieselthaler N; van der Watt GF; Wilmshurst JM
    J Child Neurol; 2010 Oct; 25(10):1288-91. PubMed ID: 20197271
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sleep problems in children with Sanfilippo syndrome.
    Colville GA; Watters JP; Yule W; Bax M
    Dev Med Child Neurol; 1996 Jun; 38(6):538-44. PubMed ID: 8647333
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.