Berardinelli A - Search Results

1

A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy.

Bonifati MD, Ruzza G, Bonometto P, Berardinelli A, Gorni K, Orcesi S, Lanzi G, Angelini C. Bonifati MD, et al. Among authors: berardinelli a. Muscle Nerve. 2000 Sep;23(9):1344-7. doi: 10.1002/1097-4598(200009)23:9<1344::aid-mus4>3.0.co;2-f. Muscle Nerve. 2000. PMID: 10951436 Clinical Trial.

2

A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspot.

Politano D, Gana S, Pezzotti E, Berardinelli A, Pasca L, Carmen Barbero V, Pichiecchio A, Maria Valente E, Errichiello E. Politano D, et al. Among authors: berardinelli a. Brain Dev. 2023 Mar;45(3):179-184. doi: 10.1016/j.braindev.2022.11.004. Epub 2022 Nov 26. Brain Dev. 2023. PMID: 36446697

3

Prospective study of gross motor development in children with SMA type II.

Bono R, Inverno M, Botteon G, Iotti E, Estienne M, Berardinelli A, Lanzi G, Fedrizzi E. Bono R, et al. Among authors: berardinelli a. Ital J Neurol Sci. 1995 May;16(4):223-30. doi: 10.1007/BF02282993. Ital J Neurol Sci. 1995. PMID: 7591674

4

Clinical and neurophysiological study in diabetic children and adolescents.

Moglia A, Lorini R, D'Annunzio G, Lanzi G, Berardinelli A, Zandrini C. Moglia A, et al. Among authors: berardinelli a. Funct Neurol. 1994 Mar-Apr;9(2):75-82. Funct Neurol. 1994. PMID: 7926890

5

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.

Tupler R, Berardinelli A, Barbierato L, Frants R, Hewitt JE, Lanzi G, Maraschio P, Tiepolo L. Tupler R, et al. Among authors: berardinelli a. J Med Genet. 1996 May;33(5):366-70. doi: 10.1136/jmg.33.5.366. J Med Genet. 1996. PMID: 8733044 Free PMC article.

6

The efficacy of noninvasive mechanical ventilation on nocturnal hypoxaemia in Duchenne's muscular dystrophy.

Fanfulla F, Berardinelli A, Gualtieri G, Zoia MC, Ottolini A, Vianello A, Lanzi G, Cerveri I. Fanfulla F, et al. Among authors: berardinelli a. Monaldi Arch Chest Dis. 1998 Feb;53(1):9-13. Monaldi Arch Chest Dis. 1998. PMID: 9632901

7

Dolicho-vertebrobasilar abnormality and migraine-like attacks.

Zambrino CA, Berardinelli A, Martelli A, Vercelli P, Termine C, Lanzi G. Zambrino CA, et al. Among authors: berardinelli a. Eur Neurol. 1999 Jan;41(1):10-4. doi: 10.1159/000007991. Eur Neurol. 1999. PMID: 9885322

8

Heart involvement in muscular dystrophies due to sarcoglycan gene mutations.

Melacini P, Fanin M, Duggan DJ, Freda MP, Berardinelli A, Danieli GA, Barchitta A, Hoffman EP, Dalla Volta S, Angelini C. Melacini P, et al. Among authors: berardinelli a. Muscle Nerve. 1999 Apr;22(4):473-9. doi: 10.1002/(sici)1097-4598(199904)22:4<473::aid-mus8>3.0.co;2-5. Muscle Nerve. 1999. PMID: 10204782

9

Response to carbamazepine of recessive-type myotonia congenita.

Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Muscle Nerve. 2000 Jan;23(1):138-9. doi: 10.1002/(sici)1097-4598(200001)23:1<138::aid-mus23>3.0.co;2-4. Muscle Nerve. 2000. PMID: 10590422 No abstract available.

10

AAEM news and comments.

Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Muscle Nerve. 2000 Jan;23(1):142-6. Muscle Nerve. 2000. PMID: 10590423 No abstract available.

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