Borrone C - Search Results

1

Borrone C, Bachmann C, Di Rocco M, Tada K, Hayasaka K, Gatti R. Borrone C, et al. J Inherit Metab Dis. 1986;9(4):402-3. doi: 10.1007/BF01800496. J Inherit Metab Dis. 1986. PMID: 3104680 No abstract available.

2

Complications of lysinuric protein intolerance must be treated with immunosuppressive drugs.

Di Rocco M, Buoncompagni A, Gattorno M, Picco P, Vignola S, Borrone C. Di Rocco M, et al. Among authors: borrone c. J Inherit Metab Dis. 1998 Aug;21(6):675-6. doi: 10.1023/a:1005440802688. J Inherit Metab Dis. 1998. PMID: 9762605 No abstract available.

3

3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease.

Di Rocco M, Caruso U, Moroni I, Lupino S, Lamantea E, Fantasia AR, Borrone C, Gibson KM. Di Rocco M, et al. Among authors: borrone c. J Inherit Metab Dis. 1999 Jun;22(5):593-8. doi: 10.1023/a:1005565610613. J Inherit Metab Dis. 1999. PMID: 10399091

4

An abnormal amino acid pattern in adenosine deaminase deficiency.

Borrone C, Di Rocco M, Caruso U, Reali S. Borrone C, et al. J Inherit Metab Dis. 1985;8 Suppl 2:119. doi: 10.1007/BF01811487. J Inherit Metab Dis. 1985. PMID: 3930857 No abstract available.

5

Neutropenia and impaired neutrophil function in glycogenosis type Ib.

Di Rocco M, Borrone C, Dallegri F, Frumento G, Patrone F. Di Rocco M, et al. Among authors: borrone c. J Inherit Metab Dis. 1984;7(4):151-4. doi: 10.1007/BF01805597. J Inherit Metab Dis. 1984. PMID: 6098781

6

Sjögren-Larsson syndrome: nuclear magnetic resonance imaging of the brain in a 4-year-old boy.

Di Rocco M, Filocamo M, Tortori-Donati P, Veneselli E, Borrone C, Rizzo WB. Di Rocco M, et al. Among authors: borrone c. J Inherit Metab Dis. 1994;17(1):112-4. doi: 10.1007/BF00735407. J Inherit Metab Dis. 1994. PMID: 8051916 No abstract available.

7

Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency.

Caimi L, Tettamanti G, Berra B, Omodeo Sale F, Borrone C, Gatti R, Durand P, Martin JJ. Caimi L, et al. Among authors: borrone c. J Inherit Metab Dis. 1982;5(4):218-24. doi: 10.1007/BF02179146. J Inherit Metab Dis. 1982. PMID: 6820444

8

Genetical and biochemical studies of two variants of fucosidosis.

Gatti R, Borrone C, Durand P. Gatti R, et al. Among authors: borrone c. Biochem Exp Biol. 1977;13(1):27-30. Biochem Exp Biol. 1977. PMID: 614046 No abstract available.

9

Fucosidosis in Calabria: founder effect or high gene frequency.

Romeo G, Borrone C, Gatti R, Durand P. Romeo G, et al. Among authors: borrone c. Lancet. 1977 Feb 12;1(8007):368-9. doi: 10.1016/s0140-6736(77)91175-8. Lancet. 1977. PMID: 64894 No abstract available.

10

Metabolic defect in arthrogryposis multiplex congenita with renal and hepatic abnormalities.

DiRocco M, Borrone C. DiRocco M, et al. Among authors: borrone c. J Pediatr. 1991 May;118(5):828-9. doi: 10.1016/s0022-3476(05)80068-x. J Pediatr. 1991. PMID: 2019948 No abstract available.

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