Andria G - Search Results

1

Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.

Ballabio A, Parenti G, Napolitano E, Di Natale P, Andria G. Ballabio A, et al. Among authors: andria g. Hum Genet. 1985;70(4):315-7. doi: 10.1007/BF00295367. Hum Genet. 1985. PMID: 3860470

2

X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene.

Ballabio A, Parenti G, Carrozzo R, Coppa G, Felici L, Migliori V, Silengo M, Franceschini P, Andria G. Ballabio A, et al. Among authors: andria g. Clin Genet. 1988 Jul;34(1):31-7. doi: 10.1111/j.1399-0004.1988.tb02612.x. Clin Genet. 1988. PMID: 3165728

3

Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.

Ballabio A, Sebastio G, Carrozzo R, Parenti G, Piccirillo A, Persico MG, Andria G. Ballabio A, et al. Among authors: andria g. Hum Genet. 1987 Dec;77(4):338-41. doi: 10.1007/BF00291422. Hum Genet. 1987. PMID: 3480263

4

X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.

Ballabio A, Parenti G, Tippett P, Mondello C, Di Maio S, Tenore A, Andria G. Ballabio A, et al. Among authors: andria g. Hum Genet. 1986 Mar;72(3):237-40. doi: 10.1007/BF00291885. Hum Genet. 1986. PMID: 3007328

5

Studies on cross-reacting material to steroid sulphatase in fibroblasts from patients affected by different types of steroid sulphatase deficiency.

Parenti G, Ballabio A, Hoogeveen AT, Van der Loos CM, Jobsis AC, Andria G. Parenti G, et al. Among authors: andria g. J Inherit Metab Dis. 1987;10(3):224-8. doi: 10.1007/BF01800065. J Inherit Metab Dis. 1987. PMID: 3123779

6

More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia.

Andria G, Ballabio A, Parenti G. Andria G, et al. Ann Neurol. 1988 Jan;23(1):103. doi: 10.1002/ana.410230124. Ann Neurol. 1988. PMID: 3422798 No abstract available.

7

Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.

Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G, et al. Ballabio A, et al. Among authors: andria g. Proc Natl Acad Sci U S A. 1987 Jul;84(13):4519-23. doi: 10.1073/pnas.84.13.4519. Proc Natl Acad Sci U S A. 1987. PMID: 3474618 Free PMC article.

8

X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia.

Andria G, Ballabio A, Parenti G. Andria G, et al. Ann Neurol. 1987 Jul;22(1):98-9. doi: 10.1002/ana.410220130. Ann Neurol. 1987. PMID: 3477126 No abstract available.

9

Steroid sulphatase deficiency is present in patients with the syndrome 'ichthyosis and male hypogonadism' and with 'Rud syndrome'.

Andria G, Ballabio A, Parenti G, Di Maio S, Piccirillo A. Andria G, et al. J Inherit Metab Dis. 1984;7 Suppl 2:159-60. doi: 10.1007/978-94-009-5612-4_54. J Inherit Metab Dis. 1984. PMID: 6434878 No abstract available.

10

Steroid sulphatase deficiency and hypogonadism.

Andria G, Ballabio A, Parenti G, DiMaio S, Piccirillo A. Andria G, et al. Eur J Pediatr. 1984 Sep;142(4):304-5. doi: 10.1007/BF00540260. Eur J Pediatr. 1984. PMID: 6489382 No abstract available.

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