Kinali M - Search Results

1

Pilot trial of salbutamol in central core and multi-minicore diseases.

Messina S, Hartley L, Main M, Kinali M, Jungbluth H, Muntoni F, Mercuri E. Messina S, et al. Among authors: kinali m. Neuropediatrics. 2004 Oct;35(5):262-6. doi: 10.1055/s-2004-821173. Neuropediatrics. 2004. PMID: 15534757 Clinical Trial.

2

Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.

Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F. Mercuri E, et al. Among authors: kinali m. Neuropediatrics. 2002 Feb;33(1):10-4. doi: 10.1055/s-2002-23593. Neuropediatrics. 2002. PMID: 11930270

3

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study.

Mercuri E, Yuva Y, Brown SC, Brockington M, Kinali M, Jungbluth H, Feng L, Sewry CA, Muntoni F. Mercuri E, et al. Among authors: kinali m. Neurology. 2002 May 14;58(9):1354-9. doi: 10.1212/wnl.58.9.1354. Neurology. 2002. PMID: 12011280

4

Pilot trial of albuterol in spinal muscular atrophy.

Kinali M, Mercuri E, Main M, De Biasia F, Karatza A, Higgins R, Banks LM, Manzur AY, Muntoni F. Kinali M, et al. Neurology. 2002 Aug 27;59(4):609-10. doi: 10.1212/wnl.59.4.609. Neurology. 2002. PMID: 12196659 Clinical Trial.

5

An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy.

Kinali M, Mercuri E, Main M, Muntoni F, Dubowitz V. Kinali M, et al. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S169-74. doi: 10.1016/s0960-8966(02)00097-4. Neuromuscul Disord. 2002. PMID: 12206813 Clinical Trial.

6

Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy.

Dubowitz V, Kinali M, Main M, Mercuri E, Muntoni F. Dubowitz V, et al. Among authors: kinali m. Eur J Paediatr Neurol. 2002;6(3):153-9. doi: 10.1053/ejpn.2002.0583. Eur J Paediatr Neurol. 2002. PMID: 12363102

7

Fracture prevalence in Duchenne muscular dystrophy.

McDonald DG, Kinali M, Gallagher AC, Mercuri E, Muntoni F, Roper H, Jardine P, Jones DH, Pike MG. McDonald DG, et al. Among authors: kinali m. Dev Med Child Neurol. 2002 Oct;44(10):695-8. doi: 10.1017/s0012162201002778. Dev Med Child Neurol. 2002. PMID: 12418795 Free article.

8

Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype.

Mercuri E, Cini C, Pichiecchio A, Allsop J, Counsell S, Zolkipli Z, Messina S, Kinali M, Brown SC, Jimenez C, Brockington M, Yuva Y, Sewry CA, Muntoni F. Mercuri E, et al. Among authors: kinali m. Neuromuscul Disord. 2003 Sep;13(7-8):554-8. doi: 10.1016/s0960-8966(03)00091-9. Neuromuscul Disord. 2003. PMID: 12921792

9

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study.

Mercuri E, Messina S, Kinali M, Cini C, Longman C, Battini R, Cioni G, Muntoni F. Mercuri E, et al. Among authors: kinali m. Neuromuscul Disord. 2004 Feb;14(2):125-9. doi: 10.1016/j.nmd.2003.09.005. Neuromuscul Disord. 2004. PMID: 14733958

10

Pilot trial of phenylbutyrate in spinal muscular atrophy.

Mercuri E, Bertini E, Messina S, Pelliccioni M, D'Amico A, Colitto F, Mirabella M, Tiziano FD, Vitali T, Angelozzi C, Kinali M, Main M, Brahe C. Mercuri E, et al. Among authors: kinali m. Neuromuscul Disord. 2004 Feb;14(2):130-5. doi: 10.1016/j.nmd.2003.11.006. Neuromuscul Disord. 2004. PMID: 14733959 Clinical Trial.

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