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Page 1
Infantile sialic acid storage disease: biochemical studies.
Berra B, Gornati R, Rapelli S, Gatti R, Mancini GM, Ciana G, Bembi B. Berra B, et al. Among authors: bembi b. Am J Med Genet. 1995 Jul 31;58(1):24-31. doi: 10.1002/ajmg.1320580107. Am J Med Genet. 1995. PMID: 7573152
ALP isoenzyme separation in type 1 Gaucher disease.
Ciana G, Tamaro G, Martini C, Ceschel S, Cuttini M, Bembi B. Ciana G, et al. Among authors: bembi b. Clin Chem Lab Med. 2000 May;38(5):479-80. doi: 10.1515/CCLM.2000.069. Clin Chem Lab Med. 2000. PMID: 10952233 No abstract available.
Response of Gaucher bone disease to enzyme replacement therapy.
Poll LW, Maas M, Terk MR, Roca-Espiau M, Bembi B, Ciana G, Weinreb NJ. Poll LW, et al. Among authors: bembi b. Br J Radiol. 2002;75 Suppl 1:A25-36. doi: 10.1259/bjr.75.suppl_1.750025. Br J Radiol. 2002. PMID: 12036830 Review.
Bone complications in children with Gaucher disease.
Bembi B, Ciana G, Mengel E, Terk MR, Martini C, Wenstrup RJ. Bembi B, et al. Br J Radiol. 2002;75 Suppl 1:A37-44. doi: 10.1259/bjr.75.suppl_1.750037. Br J Radiol. 2002. PMID: 12036831 Review.
Bone marker alterations in patients with type 1 Gaucher disease.
Ciana G, Martini C, Leopaldi A, Tamaro G, Katouzian F, Ronfani L, Bembi B. Ciana G, et al. Among authors: bembi b. Calcif Tissue Int. 2003 Mar;72(3):185-9. doi: 10.1007/s00223-001-2072-0. Epub 2003 Jan 15. Calcif Tissue Int. 2003. PMID: 12522660
161 results