Bado M - Search Results

1

Primary adrenal insufficiency in a child with a mitochondrial DNA deletion.

Bruno C, Minetti C, Tang Y, Magalhães PJ, Santorelli FM, Shanske S, Bado M, Cordone G, Gatti R, DiMauro S. Bruno C, et al. Among authors: bado m. J Inherit Metab Dis. 1998 Apr;21(2):155-61. doi: 10.1023/a:1005347826664. J Inherit Metab Dis. 1998. PMID: 9584267

2

Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria.

Bruno C, Minetti C, Shanske S, Morreale G, Bado M, Cordone G, DiMauro S. Bruno C, et al. Among authors: bado m. Neurology. 1998 Jan;50(1):296-8. doi: 10.1212/wnl.50.1.296. Neurology. 1998. PMID: 9443500

3

A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.

Bruno C, DiRocco M, Lamba LD, Bado M, Marino C, Tsujino S, Shanske S, Stella G, Minetti C, van Diggelen OP, DiMauro S. Bruno C, et al. Among authors: bado m. Neuromuscul Disord. 1999 Oct;9(6-7):403-7. doi: 10.1016/s0960-8966(99)00040-1. Neuromuscul Disord. 1999. PMID: 10545044

4

Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion.

Bruno C, Gandullia P, Santorelli FM, Biedi C, Carbone I, Bado M, Gatti R, Minetti C. Bruno C, et al. Among authors: bado m. Clin Genet. 2002 Jun;61(6):465-7. doi: 10.1034/j.1399-0004.2002.610612.x. Clin Genet. 2002. PMID: 12121356 No abstract available.

5

Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.

Bruno C, Sacco O, Santorelli FM, Assereto S, Tonoli E, Bado M, Rossi GA, Minetti C. Bruno C, et al. Among authors: bado m. J Child Neurol. 2003 Apr;18(4):300-3. doi: 10.1177/08830738030180040401. J Child Neurol. 2003. PMID: 12760436

6

Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene.

Bruno C, Santorelli FM, Assereto S, Tonoli E, Tessa A, Traverso M, Scapolan S, Bado M, Tedeschi S, Minetti C. Bruno C, et al. Among authors: bado m. Muscle Nerve. 2003 Oct;28(4):508-11. doi: 10.1002/mus.10429. Muscle Nerve. 2003. PMID: 14506725

7

Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuria.

Bruno C, Bado M, Minetti C, Cordone G, DiMauro S. Bruno C, et al. Among authors: bado m. J Child Neurol. 2000 Jun;15(6):390-3. doi: 10.1177/088307380001500607. J Child Neurol. 2000. PMID: 10868782

8

Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria.

Minetti C, Garavaglia B, Bado M, Invernizzi F, Bruno C, Rimoldi M, Pons R, Taroni F, Cordone G. Minetti C, et al. Among authors: bado m. Neuromuscul Disord. 1998 Feb;8(1):3-6. doi: 10.1016/s0960-8966(97)00121-1. Neuromuscul Disord. 1998. PMID: 9565984

9

Forearm semi-ischemic exercise test in pediatric patients.

Bruno C, Bado M, Minetti C, Cordone G. Bruno C, et al. Among authors: bado m. J Child Neurol. 1998 Jun;13(6):288-90. doi: 10.1177/088307389801300610. J Child Neurol. 1998. PMID: 9660514 No abstract available.

10

[Congenital myopathies].

Cordone G, Bado M, Minetti C. Cordone G, et al. Among authors: bado m. Minerva Pediatr. 1991 Mar;43(3):71-80. Minerva Pediatr. 1991. PMID: 1870529 Italian. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

48 results

Search Page

Filters