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Literaturhinweise: A - C

Aufzählung Akhtar S, Tullo A, Caterson B, Davies JR, Bennett K, Meek KM (2002)
Clinical and morphological features including expression of betaig-h3 and keratan sulphate proteoglycans in Maroteaux-Lamy syndrome type B and in normal cornea. Br J Ophthalmol 86:147-151.

Aufzählung Barone R, Parano E, Trifiletti RR, Fiumara A, Pavone P (2002)
White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: characterization by MRI. J Neurol Sci 195:171-175.

Aufzählung Bax MC, Colville GA (1995)
Behaviour in mucopolysaccharide disorders. Arch Dis Child 73:77-81.

Aufzählung Baxter MA, Wynn RF, Deakin JA, Bellantuono I, Edington KG, Cooper A, Besley GT, Church HJ, Wraith JE, Carr TF, Fairbairn LJ (2002)
Retrovirally mediated correction of bone marrow-derived mesenchymal stem cells from patients with mucopolysaccharidosis type I. Blood 99:1857-1859.

Aufzählung Benedik-Dolnicar M, Strmecki L, Paschke E, Steglich C, Kranjc O, Komel R (2002)
Haemophilia a and mucopolysaccharidosis I-h (hurler syndrome): a case report. Haematologica 87:ECR30.

Aufzählung Bradford TM, Litjens T, Parkinson EJ, Hopwood JJ, Brooks DA (2002)
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network. Biochemistry 41:4962-4971.

Aufzählung Brama I, Gay I, Feinmesser R, Springer C (1986)
Upper airway obstruction in Hunter syndrome. Int J Pediatr Otorhinolaryngol 11:229-235.

Aufzählung Brooks AI, Stein CS, Hughes SM, Heth J, McCray PM, Jr., Sauter SL, Johnston JC, Cory-Slechta DA, Federoff HJ, Davidson BL (2002)
Functional correction of established central nervous system deficits in an animal model of lysosomal storage disease with feline immunodeficiency virusbased vectors. Proc Natl Acad Sci U S A 99:6216-6221.

Aufzählung Buchet D, Serguera C, Zennou V, Charneau P, Mallet J (2002)
Long-term expression of beta-glucuronidase by genetically modified human neural progenitor cells grafted into the mouse central nervous system. Mol Cell Neurosci 19:389-401.

Aufzählung Bunge S, Kleijer WJ, Steglich C, Beck M, Schwinger E, Gal A (1995)
Mucopolysaccharidosis type I: identification of 13 novel mutations of the alpha- L-iduronidase gene. Hum Mutat 6:91-94.

Aufzählung Colville GA, Watters JP, Yule W, Bax M (1996)
Sleep problems in children with Sanfilippo syndrome. Dev Med Child Neurol 38:538-544.

Aufzählung Crawley AC, Niedzielski KH, Isaac EL, Davey RC, Byers S, Hopwood JJ (1997)
Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VI. J Clin Invest 99:651-662

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