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 *

94 related articles for article (PubMed ID: 8497333)

  • 21. Tachypnea of infancy as the first sign of Sanfilippo syndrome.
    Chiang J; Raiman J; Cutz E; Solomon M; Dell S
    Pediatrics; 2014 Sep; 134(3):e884-8. PubMed ID: 25113300
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Anaestethic problems in Sanfilippo syndrome. A rare case of adult patient.
    Ingrosso M; Picilli MM; Capasso A; Cecere F; Cirillo V; Merolla V
    Minerva Anestesiol; 2003; 69(7-8):641-3, 644-5. PubMed ID: 14564245
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mild Sanfilippo syndrome: a further cause of hyperactivity and behavioural disturbance.
    Wraith JE; Danks DM; Rogers JG
    Med J Aust; 1987 Nov; 147(9):450-1. PubMed ID: 3118155
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Fine structural and cytochemical findings in Sanfilippo's disease type A (author's transl)].
    Cain H; Egner E; Kresse H
    Verh Dtsch Ges Pathol; 1976; ():270-3. PubMed ID: 828815
    [No Abstract]   [Full Text] [Related]  

  • 25. Type III D mucopolysaccharidosis (Sanfilippo D): clinical course and symptoms.
    Tylki-Szymańska A; Czartoryska B; Górska D; Piesiewicz-Grzonkowska E
    Acta Paediatr Jpn; 1998 Oct; 40(5):492-4. PubMed ID: 9821715
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Sanfilippo's syndrome].
    Orii T
    Nihon Rinsho; 1977; 35 Suppl 1():1068-9. PubMed ID: 418202
    [No Abstract]   [Full Text] [Related]  

  • 27. [Characteristics of urinary heparan sulfate in 5 cases of Sanfilippo's syndrome].
    Fossati G; Sinigaglia F; Calatroni A
    Boll Soc Ital Biol Sper; 1974 Oct; 50(19):1552-8. PubMed ID: 4282024
    [No Abstract]   [Full Text] [Related]  

  • 28. [Sanfilippo's disease: clinico-genetic and biological study of 2 families].
    Carlomagno S; Federico A; Vitiello F; Pinto L; Vertucci P; Marolda M; Balbi R; Guazzi GC
    Acta Neurol (Napoli); 1974; 29(3):231-51. PubMed ID: 4213902
    [No Abstract]   [Full Text] [Related]  

  • 29. From hypertransaminasemia to mucopolysaccharidosis IIIA.
    Krawiec P; Pac-Kożuchowska E; Mełges B; Mroczkowska-Juchkiewicz A; Skomra S; Pawłowska-Kamieniak A; Kominek K
    Ital J Pediatr; 2014 Dec; 40():97. PubMed ID: 25439061
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family].
    Nobili B; Iolascon A; Bello L; Chianese C; Rasulo V; Iolascon G; Pinto L
    Pediatria (Napoli); 1983; 91(2-3):295-301. PubMed ID: 6420769
    [No Abstract]   [Full Text] [Related]  

  • 31. [Changes in urinary acid oligosaccharides after transfusion of normal plasma in 2 cases of Sanfilippo's syndrome].
    Mainardi E; Moretti M; Calatroni A
    Boll Soc Ital Biol Sper; 1974 Oct; 50(19):1540-6. PubMed ID: 4218490
    [No Abstract]   [Full Text] [Related]  

  • 32. Musculoskeletal manifestations of Sanfilippo Syndrome (mucopolysaccharidosis type III).
    White KK; Karol LA; White DR; Hale S
    J Pediatr Orthop; 2011; 31(5):594-8. PubMed ID: 21654471
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Mucopolysaccharidosis type 3 (Sanfilippo's syndrome). A cause of progressive mental retardation].
    Börjeson M; Heinegård D; Ockerman PA
    Nord Med; 1969 May; 81(18):567-9. PubMed ID: 4238726
    [No Abstract]   [Full Text] [Related]  

  • 34. [Sanfilippo's syndrome: typing of mucopolisaccharides in urine and enzymatic determination in plasma].
    Burrows R; Muzzo S
    Rev Chil Pediatr; 1980; 51(2):129-33. PubMed ID: 6448458
    [No Abstract]   [Full Text] [Related]  

  • 35. [Sanfilippo's syndrome].
    Higami S; Tanaka A
    Nihon Rinsho; 1978 May; Suppl():1408-9. PubMed ID: 99543
    [No Abstract]   [Full Text] [Related]  

  • 36. Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing clinicians.
    Fraser J; Wraith JE; Delatycki MB
    Clin Genet; 2002 Nov; 62(5):418-21. PubMed ID: 12431260
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Hypothyroidism : diagnostic error and sequenlae. Report of a case].
    Lernet P
    Padiatr Padol; 1975; 10(1):81-7. PubMed ID: 1124213
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical and neuroradiological follow-up in mucopolysaccharidosis type III (Sanfilippo syndrome).
    Barone R; Nigro F; Triulzi F; Musumeci S; Fiumara A; Pavone L
    Neuropediatrics; 1999 Oct; 30(5):270-4. PubMed ID: 10598840
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Differences in the nonreducing ends of heparan sulfates excreted by patients with mucopolysaccharidoses revealed by bacterial heparitinases: a new tool for structural studies and differential diagnosis of Sanfilippo's and Hunter's syndromes.
    Toma L; Dietrich CP; Nader HB
    Lab Invest; 1996 Dec; 75(6):771-81. PubMed ID: 8973472
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Toxoplasmin skin sensitivity in the mother and child among cases of mental retardation in Iraq.
    Amin-Zaki L; al-Saffar G; al-Aswad B
    Folia Parasitol (Praha); 1971; 18(2):179-82. PubMed ID: 5163215
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.