Bertini E - Search Results

1

X-linked adrenoleukodystrophy: first report of the Italian Study Group.

Di Biase A, Salvati S, Avellino C, Cappa M, Bertini E, Moroni I, Rimoldi M, Uziel G. Di Biase A, et al. Among authors: bertini e. Ital J Neurol Sci. 1998 Oct;19(5):315-9. doi: 10.1007/BF00713859. Ital J Neurol Sci. 1998. PMID: 10933453

2

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency.

Bertini E, Dionisi-Vici C, Garavaglia B, Burlina AB, Sabatelli M, Rimoldi M, Bartuli A, Sabetta G, DiDonato S. Bertini E, et al. Eur J Pediatr. 1992 Feb;151(2):121-6. doi: 10.1007/BF01958956. Eur J Pediatr. 1992. PMID: 1537353

3

Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathy.

Uziel G, Bertini E, Bardelli P, Rimoldi M, Gambetti M. Uziel G, et al. Among authors: bertini e. Dev Neurosci. 1991;13(4-5):274-9. doi: 10.1159/000112173. Dev Neurosci. 1991. PMID: 1817033 Clinical Trial.

4

[Neuroendocrine changes in adrenoleukodystrophy (ALD). Their relationship with new therapeutic strategies].

Cappa M, Lancia A, Cambiaso P, Del Balzo P, Di Capua M, Danielli E, Gambetti M, Bertini E. Cappa M, et al. Among authors: bertini e. Minerva Pediatr. 1991 Mar;43(3):125-6. Minerva Pediatr. 1991. PMID: 1870506 Italian. No abstract available.

5

[Diet therapy with erucic acid in patients with X-linked adrenoleukodystrophy].

Uziel G, Bertini E, Bardelli P, Rimoldi M, Gambetti M. Uziel G, et al. Among authors: bertini e. Minerva Pediatr. 1991 Mar;43(3):127-31. Minerva Pediatr. 1991. PMID: 1870507 Italian. No abstract available.

6

A new therapeutic approach for X-linked adrenoleukodystrophy.

Cappa M, Bertini E, Di Capua M, Rimoldi M, Uziel G. Cappa M, et al. Among authors: bertini e. Eur J Pediatr. 1990 May;149(8):595-6. doi: 10.1007/BF01957704. Eur J Pediatr. 1990. PMID: 2347360 No abstract available.

7

High dose immunoglobulin IV treatment in adrenoleukodystrophy.

Cappa M, Bertini E, del Balzo P, Cambiaso P, Di Biase A, Salvati S. Cappa M, et al. Among authors: bertini e. J Neurol Neurosurg Psychiatry. 1994 Nov;57 Suppl(Suppl):69-70; discussion 71. doi: 10.1136/jnnp.57.suppl.69. J Neurol Neurosurg Psychiatry. 1994. PMID: 7964860 Free PMC article. Clinical Trial.

8

Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family.

Manfredi G, Silvestri G, Servidei S, Ricci E, Mirabella M, Bertini E, Papacci M, Rana M, Tonali P. Manfredi G, et al. Among authors: bertini e. J Neurol Sci. 1993 Mar;115(1):91-4. doi: 10.1016/0022-510x(93)90071-6. J Neurol Sci. 1993. PMID: 8468596

9

Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patients.

Caruso U, Adami A, Bertini E, Burlina AB, Carnevale F, Cerone R, Dionisi-Vici C, Giordano G, Leuzzi E, Parenti G, Savasta S, Uziel G, Zeviani M. Caruso U, et al. Among authors: bertini e. J Inherit Metab Dis. 1996;19(2):143-8. doi: 10.1007/BF01799415. J Inherit Metab Dis. 1996. PMID: 8739951 Review. No abstract available.

10

Neurophysiological abnormalities in adrenoleukodystrophy carriers. Evidence of different degrees of central nervous system involvement.

Restuccia D, Di Lazzaro V, Valeriani M, Oliviero A, Le Pera D, Colosimo C, Burdi N, Cappa M, Bertini E, Di Biase A, Tonali P. Restuccia D, et al. Among authors: bertini e. Brain. 1997 Jul;120 ( Pt 7):1139-48. doi: 10.1093/brain/120.7.1139. Brain. 1997. PMID: 9236627

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