Romeo G - Search Results

1

X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms.

Romeo G, Rocchi M, Roncuzzi L, Ferlini A, Nobile C, Rugolo M. Romeo G, et al. Adv Neurol. 1988;48:31-6. Adv Neurol. 1988. PMID: 2891257 Review. No abstract available.

2

Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies.

Romeo G, Devoto M, Archidiacono N, Ferlini A, Roncuzzi L, Melis MA, Paderi E, Ferrari M, Tedeschi S, Galluzzi G, et al. Romeo G, et al. Eur J Pediatr. 1988 May;147(4):412-5. doi: 10.1007/BF00496422. Eur J Pediatr. 1988. PMID: 3165066

3

Partial digestion with restriction enzymes of ultraviolet-irradiated human genomic DNA: a method for identifying restriction site polymorphisms.

Nobile C, Romeo G. Nobile C, et al. Among authors: romeo g. Genomics. 1988 Oct;3(3):272-4. doi: 10.1016/0888-7543(88)90088-2. Genomics. 1988. PMID: 2906329

4

Discrimination of peripheral polyneuropathies caused by TTR variant or diabetes in the same pedigree through protein studies.

Ferlini A, Romeo G, Tassinari CA, Saraiva MJ, Costa PP, Salvi F. Ferlini A, et al. Among authors: romeo g. Adv Neurol. 1988;48:201-8. Adv Neurol. 1988. PMID: 3334782 No abstract available.

5

Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees.

Romeo G, Roncuzzi L, Sangiorgi S, Giacanelli M, Liguori M, Tessarolo D, Rocchi M. Romeo G, et al. Hum Genet. 1988 Sep;80(1):59-62. doi: 10.1007/BF00451457. Hum Genet. 1988. PMID: 3417305

6

[New instruments in molecular genetics for the prevention of X chromosome-linked muscular dystrophy].

Ferlini A, Roncuzzi L, Romeo G. Ferlini A, et al. Among authors: romeo g. Minerva Pediatr. 1986 Aug 31;38(15-16):639-42. Minerva Pediatr. 1986. PMID: 3796513 Italian. No abstract available.

7

Increased chloride efflux in fibroblasts from X-linked muscular dystrophies and clones from Duchenne carriers.

Rugolo M, Rocchi M, Lenaz G, Romeo G. Rugolo M, et al. Among authors: romeo g. FEBS Lett. 1987 Feb 23;212(2):313-6. doi: 10.1016/0014-5793(87)81367-4. FEBS Lett. 1987. PMID: 3817163 Free article.

8

Origin of new mutations in Duchenne muscular dystrophy.

Roncuzzi L, Ferlini A, Pirozzi A, Romeo G. Roncuzzi L, et al. Among authors: romeo g. Hum Genet. 1986 Dec;74(4):456-60. doi: 10.1007/BF00280507. Hum Genet. 1986. PMID: 2878873

9

A second genetic locus for autosomal dominant polycystic kidney disease.

Romeo G, Devoto M, Costa G, Roncuzzi L, Catizone L, Zucchelli P, Germino GG, Keith T, Weatherall DJ, Reeders ST. Romeo G, et al. Lancet. 1988 Jul 2;2(8601):8-11. doi: 10.1016/s0140-6736(88)92943-1. Lancet. 1988. PMID: 2898665

10

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G. Archidiacono N, et al. Among authors: romeo g. Hum Genet. 1991 Apr;86(6):604-6. doi: 10.1007/BF00201549. Hum Genet. 1991. PMID: 1673961

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,002 results

Search Page

Filters