Cetta G - Search Results

1

Biochemical, morphological and stereological study of the dermis in three members of a large family with type IV Ehlers-Danlos syndrome.

Vitellaro-Zuccarello L, Dyne K, Cetta G. Vitellaro-Zuccarello L, et al. Among authors: cetta g. Connect Tissue Res. 1989;23(1):1-17. doi: 10.3109/03008208909103900. Connect Tissue Res. 1989. PMID: 2632142

2

Low levels of serum type III procollagen aminoterminal propeptide confirmed type III collagen deficiency in patients without typical clinical symptoms of Ehlers-Danlos type IV.

Dyne KM, Zanaboni G, Annoni G, De Agostini MP, Cetta G. Dyne KM, et al. Among authors: cetta g. Eur J Clin Invest. 1989 Aug;19(4):362-6. doi: 10.1111/j.1365-2362.1989.tb00242.x. Eur J Clin Invest. 1989. PMID: 2506053

3

Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.

Cetta G, Rossi A, Tenni R, Valli M, Forlino A, Zanaboni G, Dyne K, Burgio GR. Cetta G, et al. Connect Tissue Res. 1993;29(1):41-9. doi: 10.3109/03008209309061965. Connect Tissue Res. 1993. PMID: 8339545

4

Ehlers-Danlos syndrome type VIII: biochemical, stereological and immunocytochemical studies on dermis from a child with clinical signs of Ehlers-Danlos syndrome and a family history of premature loss of permanent teeth.

Dyne KM, Vitellaro-Zuccarello L, Bacchella L, Lanzi G, Cetta G. Dyne KM, et al. Among authors: cetta g. Br J Dermatol. 1993 Apr;128(4):458-63. doi: 10.1111/j.1365-2133.1993.tb00211.x. Br J Dermatol. 1993. PMID: 8494762

5

[Ehlers-Danlos syndrome. Description of 2 clinical cases].

Ottolini A, Berardinelli A, Besana D, Cetta G, Dyne KM, Lanzi G. Ottolini A, et al. Among authors: cetta g. Minerva Pediatr. 1992 May;44(5):231-6. Minerva Pediatr. 1992. PMID: 1620075 Italian.

6

Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta.

Tenni R, Biglino P, Dyne K, Rossi A, Filocamo M, Pendola F, Brunelli P, Buttitta P, Borrone C, Cetta G. Tenni R, et al. Among authors: cetta g. J Inherit Metab Dis. 1991;14(2):189-201. doi: 10.1007/BF01800591. J Inherit Metab Dis. 1991. PMID: 1886404

7

Marfan syndrome: a collagen disorder?

Zanaboni G, De Agostini MP, Valli M, Dyne K, Cetta G, Hollister DW, Castellani AA. Zanaboni G, et al. Among authors: cetta g. Ital J Biochem. 1989 Jul-Aug;38(4):288A-289A. Ital J Biochem. 1989. PMID: 2583982 No abstract available.

8

Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity.

Tenni R, Cetta G, Dyne K, Valli M, Zanaboni G, Castellani AA. Tenni R, et al. Among authors: cetta g. Ann N Y Acad Sci. 1988;543:73-82. doi: 10.1111/j.1749-6632.1988.tb55317.x. Ann N Y Acad Sci. 1988. PMID: 3214054 No abstract available.

9

Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. Defective pro-alpha 1(I) chains in a patient with abnormal proteoglycan metabolism and mineral deposits in the dermis.

Tenni R, Cetta G, Dyne K, Rossi A, Quacci D, Lenzi L, Castellani AA. Tenni R, et al. Among authors: cetta g. Hum Genet. 1988 Jul;79(3):245-50. doi: 10.1007/BF00366245. Hum Genet. 1988. PMID: 3402997

10

Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta.

Dyne K, Cetta G, Tenni R, Rossi A, Finardi E, Brunelli PC, Castellani AA. Dyne K, et al. Among authors: cetta g. Ital J Biochem. 1987 Jul-Aug;36(4):256-66. Ital J Biochem. 1987. PMID: 3429209

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