BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 30503158)

  • 21. MPS I: Early diagnosis, bone disease and treatment, where are we now?
    Kingma SDK; Jonckheere AI
    J Inherit Metab Dis; 2021 Nov; 44(6):1289-1310. PubMed ID: 34480380
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Frequency of Carpal Tunnel Syndrome in Hurler Syndrome After Peritransplant Enzyme Replacement Therapy: A Retrospective Comparison.
    Wyffels ML; Orchard PJ; Shanley RM; Miller WP; Van Heest AE
    J Hand Surg Am; 2017 Jul; 42(7):573.e1-573.e8. PubMed ID: 28479223
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Treatment of 2 children with mucopolysaccharidosis by allogeneic hematopoietic stem cell transplantation].
    Chen J; Jiang H; Dong L; Wang Y; Luo C; Zhou M; Zhang W; Huang S; Gu X; Qiu W; Zhang H; Gu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):675-7. PubMed ID: 19065530
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy.
    Furlan F; Rovelli A; Rigoldi M; Filocamo M; Tappino B; Friday D; Gasperini S; Mariani S; Izzi C; Bondioni MP; Gellera C; Venerando A; Villa N; Del Carmen Rodriguez Perez M; Pavan F; Biondi A; Parini R
    Ital J Pediatr; 2018 Nov; 44(Suppl 2):128. PubMed ID: 30442200
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Outcome in six children with mucopolysaccharidosis type IH, Hurler syndrome, after haematopoietic stem cell transplantation (HSCT).
    Malm G; Gustafsson B; Berglund G; Lindström M; Naess K; Borgström B; von Döbeln U; Ringdén O
    Acta Paediatr; 2008 Aug; 97(8):1108-12. PubMed ID: 18452566
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The natural history of neurocognition in MPS disorders: A review.
    Shapiro EG; Eisengart JB
    Mol Genet Metab; 2021 May; 133(1):8-34. PubMed ID: 33741271
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Failure to shorten the diagnostic delay in two ultra-orphan diseases (mucopolysaccharidosis types I and III): potential causes and implications.
    Kuiper GA; Meijer OLM; Langereis EJ; Wijburg FA
    Orphanet J Rare Dis; 2018 Jan; 13(1):2. PubMed ID: 29310675
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical manifestations and treatment of mucopolysaccharidosis type I patients in Latin America as compared with the rest of the world.
    Muñoz-Rojas MV; Bay L; Sanchez L; van Kuijck M; Ospina S; Cabello JF; Martins AM
    J Inherit Metab Dis; 2011 Oct; 34(5):1029-37. PubMed ID: 21541721
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Combination of enzyme replacement and hematopoietic stem cell transplantation as therapy for Hurler syndrome.
    Tolar J; Grewal SS; Bjoraker KJ; Whitley CB; Shapiro EG; Charnas L; Orchard PJ
    Bone Marrow Transplant; 2008 Mar; 41(6):531-5. PubMed ID: 18037941
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry.
    D'Aco K; Underhill L; Rangachari L; Arn P; Cox GF; Giugliani R; Okuyama T; Wijburg F; Kaplan P
    Eur J Pediatr; 2012 Jun; 171(6):911-9. PubMed ID: 22234477
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The presenting features of mucopolysaccharidosis type IH (Hurler syndrome).
    Cleary MA; Wraith JE
    Acta Paediatr; 1995 Mar; 84(3):337-9. PubMed ID: 7780260
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The evolution of pulmonary function in childhood onset Mucopolysaccharidosis type I.
    Broomfield A; Sims J; Mercer J; Hensman P; Ghosh A; Tylee K; Stepien KM; Oldham A; Prathivadi Bhayankaram N; Wynn R; Wright NB; Jones SA; Wilkinson S
    Mol Genet Metab; 2021 Feb; 132(2):94-99. PubMed ID: 32713717
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome.
    Bijarnia S; Shaw P; Vimpani A; Smith R; Pacey V; O'Grady H; Christodoulou J; Sillence D
    J Paediatr Child Health; 2009; 45(7-8):469-72. PubMed ID: 19712183
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enzyme replacement therapy in mucopolysaccharidosis type I: progress and emerging difficulties.
    Wraith JE
    J Inherit Metab Dis; 2001 Apr; 24(2):245-50. PubMed ID: 11405343
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Unexpected coronary artery findings in mucopolysaccharidosis. Report of four cases and literature review.
    Braunlin E; Orchard PJ; Whitley CB; Schroeder L; Reed RC; Manivel JC
    Cardiovasc Pathol; 2014; 23(3):145-51. PubMed ID: 24508139
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Growth and endocrine function in patients with Hurler syndrome after hematopoietic stem cell transplantation.
    Polgreen LE; Tolar J; Plog M; Himes JH; Orchard PJ; Whitley CB; Miller BS; Petryk A
    Bone Marrow Transplant; 2008 Jun; 41(12):1005-11. PubMed ID: 18278070
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Obstructive sleep apnea syndrome after hematopoietic stem cell transplantation in children with mucopolysaccharidosis type I.
    Moreau J; Brassier A; Amaddeo A; Neven B; Caillaud C; Chabli A; Fernandez-Bolanos M; Olmo J; Valayannopoulos V; Fauroux B
    Mol Genet Metab; 2015 Dec; 116(4):275-80. PubMed ID: 26602600
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Improvement in time to treatment, but not time to diagnosis, in patients with mucopolysaccharidosis type I.
    Giugliani R; Muschol N; Keenan HA; Dant M; Muenzer J
    Arch Dis Child; 2021 Jul; 106(7):674-679. PubMed ID: 33139350
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Successful treatment of severe heart failure in an infant with Hurler syndrome.
    Hirth A; Berg A; Greve G
    J Inherit Metab Dis; 2007 Oct; 30(5):820. PubMed ID: 17768668
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mortality after hematopoietic stem cell transplantation for severe mucopolysaccharidosis type I: the 30-year University of Minnesota experience.
    Rodgers NJ; Kaizer AM; Miller WP; Rudser KD; Orchard PJ; Braunlin EA
    J Inherit Metab Dis; 2017 Mar; 40(2):271-280. PubMed ID: 28054207
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.