Published in Am J Vet Res on February 01, 1988
Biomechanical assessment of the effects of decompressive surgery in non-chondrodystrophic and chondrodystrophic canine multisegmented lumbar spines. Eur Spine J (2012) 0.89
Comparison of the access window created by hemilaminectomy and mini-hemilaminectomy in the thoracolumbar vertebral canal using computed tomography. Can Vet J (2014) 0.80
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue. Brain (2008) 1.65
GNE protein expression and subcellular distribution are unaltered in HIBM. Neurology (2007) 0.94
New concepts of coxofemoral joint stability and the development of a clinical stress-radiographic method for quantitating hip joint laxity in the dog. J Am Vet Med Assoc (1990) 0.94
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes. Neurology (2002) 0.82
C283Y mutation in the gamma-sarcoglycan gene in Greek Gypsies with severe limb girdle muscular dystrophy. Eur J Neurol (2010) 0.82
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis. Neuromuscul Disord (2005) 0.82
A synonymous codon change in the LMNA gene alters mRNA splicing and causes limb girdle muscular dystrophy type 1B. J Med Genet (2003) 0.82
Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration. J Neurol (2010) 0.80
No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations. Eur J Neurol (2008) 0.80
Phenotypic variability in siblings with calpainopathy (LGMD2A). Acta Myol (2008) 0.80
Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutations. Acta Myol (2005) 0.78
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis. Lancet (1999) 0.78
Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein. Clin Neuropathol (2007) 0.76
Neurodegeneration-associated proteins and inflammation in sporadic inclusion-body myositis. Adv Exp Med Biol (2001) 0.76
LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments. Acta Myol (2006) 0.75
Prion codon 129 homozygosity and sporadic inclusion body myositis. Neurology (2001) 0.75
Chronic hypertrophic pyloric gastropathy as a cause of pyloric obstruction in the dog. J Am Vet Med Assoc (1985) 0.75
Urinary diversion. Vet Clin North Am Small Anim Pract (1984) 0.75
Use of serum beta-chain human chorionic gonadotropin in the management of testis tumor. Natl Cancer Inst Monogr (1978) 0.75
Ureterocolonic anastomosis in clinically normal dogs. Am J Vet Res (1988) 0.75
Treatment of severely comminuted diaphyseal fractures in the dog, using standard bone plates and autogenous cancellous bone graft to span fracture gaps: 11 cases (1979-1983). J Am Vet Med Assoc (1986) 0.75
Effect of sera of patients with genitourinary tract cancers on transformation of lymphocytes stimulated with anti-thymocyte globulin. Natl Cancer Inst Monogr (1978) 0.75
Vitamin B-6 metabolism as affected by exercise in trained and untrained women fed diets differing in carbohydrate and vitamin B-6 content. Am J Clin Nutr (1987) 0.75
Unique PABPN1 gene mutation in a large Bulgarian family with OPMD. J Neurol (2008) 0.75
Furosemide overdose and maximal allowable weight standards. Mil Med (1989) 0.75
Pylorectomy and gastroduodenostomy in the dog: technique and clinical results in 28 cases. J Am Vet Med Assoc (1985) 0.75