Detalhe da pesquisa
1.
De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects.
Hum Mol Genet;
26(24): 4849-4860, 2017 12 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29036646
2.
Clinical trial readiness in non-ambulatory boys and men with duchenne muscular dystrophy: MDA-DMD network follow-up.
Muscle Nerve;
54(4): 681-9, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26930423
3.
Outcome reliability in non-ambulatory boys/men with Duchenne muscular dystrophy.
Muscle Nerve;
51(4): 522-32, 2015 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25056178
4.
Acute Transverse Myelitis Caused by Echovirus 11 in a Pediatric Patient: Case Report and Review of the Current Literature.
Child Neurol Open;
5: 2329048X17751526, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29372173
5.
Infantile Epileptic Encephalopathy Associated With SCN2A Mutation Responsive to Oral Mexiletine.
Pediatr Neurol;
66: 108-111, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27867041
6.
Adoptive protection from experimental myasthenia gravis with T cells from mice treated nasally with acetylcholine receptor epitopes.
J Neuroimmunol;
123(1-2): 123-34, 2002 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-11880157
7.
One year outcome of boys with Duchenne muscular dystrophy using the Bayley-III scales of infant and toddler development.
Pediatr Neurol;
50(6): 557-63, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24842254
8.
Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network.
Neuromuscul Disord;
23(7): 529-39, 2013 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23726376