Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1955 1
1958 3
1959 3
1960 8
1961 1
1962 4
1963 12
1964 2
1965 6
1966 3
1967 10
1968 2
1969 6
1971 8
1973 3
1974 2
1975 1
1976 2
1977 3
1978 1
1979 4
1980 1
1981 1
1982 5
1983 2
1984 2
1985 4
1986 4
1988 1
1989 2
1990 2
1991 5
1992 3
1993 9
1994 2
1995 3
1996 6
1997 3
1998 4
1999 5
2001 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

151 results

Results by year

Filters applied: . Clear all
Page 1
Fucosidosis.
Durand P, Borrone C, Della Cella G. Durand P, et al. Among authors: borrone c. J Pediatr. 1969 Oct;75(4):665-74. doi: 10.1016/s0022-3476(69)80464-6. J Pediatr. 1969. PMID: 4241464 No abstract available.
[Mucopolysaccharidosis].
Durand P, Borrone C, Della Cella G, Liotta A. Durand P, et al. Among authors: borrone c. Recenti Prog Med. 1968 Mar;44(3):279-300. Recenti Prog Med. 1968. PMID: 4242464 Italian. No abstract available.
Sialidosis (mucolipidosis I).
Durand P, Gatti R, Cavalieri S, Borrone C, Tondeur M, Michalski JC, Strecker G. Durand P, et al. Among authors: borrone c. Helv Paediatr Acta. 1977 Nov;32(4-5):391-400. Helv Paediatr Acta. 1977. PMID: 617984
Diagnostic problems in congenital myotonic dystrophy.
DiRocco M, Gennarelli M, Veneselli E, Bado M, Romanengo M, Celle ME, Cordone G, Borrone C. DiRocco M, et al. Among authors: borrone c. Eur J Pediatr. 1996 Nov;155(11):995. doi: 10.1007/BF02282900. Eur J Pediatr. 1996. PMID: 8911909 No abstract available.
[FAMILIAL HYPERGAMMAGLOBULINEMIA].
BORRONE C, MASSIMO L, DEPRA M. BORRONE C, et al. Minerva Pediatr. 1963 Oct 13;15:1065-7. Minerva Pediatr. 1963. PMID: 14097701 Italian. No abstract available.
Trichothiodystrophy--BIDS, IBIDS and PIBIDS?
Crovato F, Borrone C, Rebora A. Crovato F, et al. Among authors: borrone c. Br J Dermatol. 1983 Feb;108(2):247. doi: 10.1111/j.1365-2133.1983.tb00068.x. Br J Dermatol. 1983. PMID: 6824580 No abstract available.
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
Nelson I, Degoul F, Obermaier-Kusser B, Romero N, Borrone C, Marsac C, Vayssiere JL, Gerbitz K, Fardeau M, Ponsot G, Lestienne P. Nelson I, et al. Among authors: borrone c. Nucleic Acids Res. 1989 Oct 25;17(20):8117-24. doi: 10.1093/nar/17.20.8117. Nucleic Acids Res. 1989. PMID: 2813058 Free PMC article.
Discharge report accuracy.
Rosati U, Minicucci L, Battistini E, Lattere M, Chiossi M, Pastore G, Borrone C. Rosati U, et al. Among authors: borrone c. Qual Assur Health Care. 1991;3(4):263-5. doi: 10.1093/intqhc/3.4.263. Qual Assur Health Care. 1991. PMID: 1790325
151 results