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 *

93 related articles for article (PubMed ID: 10632258)

  • 21. Hunter-Hurler Syndrome: clinical and biochemical study. Combined clinical staff conference at th National Institutes of Health.
    Dekaban A; Rennert O; Hathaway B
    Med Ann Dist Columbia; 1966 Nov; 35(11):596-602. PubMed ID: 4224139
    [No Abstract]   [Full Text] [Related]  

  • 22. Hunter syndrome.
    Shrivastva J; Mehta B
    Indian Pediatr; 2000 Aug; 37(8):908. PubMed ID: 10951649
    [No Abstract]   [Full Text] [Related]  

  • 23. Multivalvular thickening in a case of Hunter's syndrome.
    Wander GS; Sandha GS; Chawla AS; Khurana SB
    J Assoc Physicians India; 1994 Feb; 42(2):161-2. PubMed ID: 7860484
    [No Abstract]   [Full Text] [Related]  

  • 24. Hunter syndrome (MPS II-B): a report of bilateral vitreous floaters and maculopathy.
    Anawis MA
    Ophthalmic Genet; 2006 Jun; 27(2):71-2. PubMed ID: 16754210
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic counselling for Hunter syndrome.
    Epstein CJ; Yatziv S; Neufeld E; Liebaers I
    Lancet; 1976 Oct; 2(7988):737-8. PubMed ID: 61412
    [No Abstract]   [Full Text] [Related]  

  • 26. Mild form of the Hunter syndrome, indentity of the biochemical defect with the severe type.
    Wiesmann UN; Rampini S
    Helv Paediatr Acta; 1974 Apr; 29(1):73-8. PubMed ID: 4275601
    [No Abstract]   [Full Text] [Related]  

  • 27. [Follow-up of patients with Hunter syndrome: the Hunter Outcome Survey (HOS) registry].
    del Toro-Riera M
    Rev Neurol; 2007 Feb; 44 Suppl 1():S13-7. PubMed ID: 17345554
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Clinical aspects of mucopolysaccharidosis type II].
    Sanjurjo-Crespo P
    Rev Neurol; 2007 Feb; 44 Suppl 1():S3-6. PubMed ID: 17345555
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [FG syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):182-3. PubMed ID: 11057188
    [No Abstract]   [Full Text] [Related]  

  • 30. Portal hypertension in a patient with Hunter disease.
    Kato T; Isogai K; Orii K; Kuratsubo I; Kondo N; Orii T; Suzuki Y
    J Inherit Metab Dis; 2006 Oct; 29(5):686. PubMed ID: 16972178
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients.
    Ochiai T; Suzuki Y; Kato T; Shichino H; Chin M; Mugishima H; Orii T
    J Eur Acad Dermatol Venereol; 2007 Sep; 21(8):1082-5. PubMed ID: 17714129
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hydrocephalus in Hunter Syndrome.
    van Aerde J; Plets C; Van der Hauwaert L
    Acta Paediatr Belg; 1981; 34(2):93-6. PubMed ID: 6801919
    [No Abstract]   [Full Text] [Related]  

  • 33. Multidisciplinary management of Hunter syndrome.
    Muenzer J; Beck M; Eng CM; Escolar ML; Giugliani R; Guffon NH; Harmatz P; Kamin W; Kampmann C; Koseoglu ST; Link B; Martin RA; Molter DW; Muñoz Rojas MV; Ogilvie JW; Parini R; Ramaswami U; Scarpa M; Schwartz IV; Wood RE; Wraith E
    Pediatrics; 2009 Dec; 124(6):e1228-39. PubMed ID: 19901005
    [TBL] [Abstract][Full Text] [Related]  

  • 34. What syndrome is this? Hunter syndrome (mucopolysaccharidosis II).
    Panine VV; Hashimoto K
    Pediatr Dermatol; 1995 Dec; 12(4):370-2. PubMed ID: 8747590
    [No Abstract]   [Full Text] [Related]  

  • 35. [X-linked dilated cardiomyopathy: a cardiospecific phenotype of dystrophinopathy].
    Yoshida K; Takeda S
    Ryoikibetsu Shokogun Shirizu; 2001; (35):23-7. PubMed ID: 11555918
    [No Abstract]   [Full Text] [Related]  

  • 36. [Guideline for diagnosis, follow-up and treatment of mucopolysaccharidoses type II or Hunter disease].
    Grupo de Trabajo de Enfermedades poco frecuentes
    Arch Argent Pediatr; 2011 Apr; 109(2):175-81. PubMed ID: 21591474
    [No Abstract]   [Full Text] [Related]  

  • 37. [Type II mucolipidosis].
    Maroteaux P; Hors-Cayla MC; Pont J
    Presse Med (1893); 1970 Jan; 78(4):179-81. PubMed ID: 4244747
    [No Abstract]   [Full Text] [Related]  

  • 38. Hunter syndrome.
    Nurs Times; 2005 Apr 12-18; 101(15):29. PubMed ID: 15850258
    [No Abstract]   [Full Text] [Related]  

  • 39. Unrelated umbilical cord blood transplantation in infancy for mucopolysaccharidosis type IIB (Hunter syndrome) complicated by autoimmune hemolytic anemia.
    Mullen CA; Thompson JN; Richard LA; Chan KW
    Bone Marrow Transplant; 2000 May; 25(10):1093-7. PubMed ID: 10828871
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity.
    Young ID; Harper PS; Archer IM; Newcombe RG
    J Med Genet; 1982 Dec; 19(6):401-7. PubMed ID: 6818347
    [TBL] [Abstract][Full Text] [Related]  

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