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Gowers' sign revisited.
Wallace GB, Newton RW. Wallace GB, et al. Arch Dis Child. 1989 Sep;64(9):1317-9. doi: 10.1136/adc.64.9.1317. Arch Dis Child. 1989. PMID: 2817955 Free PMC article.
We studied the patterns of standing in children with neuromuscular disorders and central hypotonia for Gowers' sign, and compared these two groups with healthy controls. ...
We studied the patterns of standing in children with neuromuscular disorders and central hypotonia for Gowers' sign, and compa …
Juvenile dermatomyositis: a 20-year retrospective analysis of treatment and clinical outcomes.
Sun C, Lee JH, Yang YH, Yu HH, Wang LC, Lin YT, Chiang BL. Sun C, et al. Pediatr Neonatol. 2015 Feb;56(1):31-9. doi: 10.1016/j.pedneo.2014.02.006. Epub 2014 Jun 27. Pediatr Neonatol. 2015. PMID: 24985888 Free article.
After excluding one patient with an incomplete record, the remaining 31 patients who had muscle weakness were analyzed; among them, 22 (70.97%) achieved complete clinical response, but only six (19.4%) achieved complete clinical remission. Multivariate analysis showed that female …
After excluding one patient with an incomplete record, the remaining 31 patients who had muscle weakness were analyzed; among them, 22 (70.9 …
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional study.
Caria F, Cescon M, Gualandi F, Pichiecchio A, Rossi R, Rimessi P, Cotti Piccinelli S, Gallo Cassarino S, Gregorio I, Galvagni A, Ferlini A, Padovani A, Bonaldo P, Filosto M. Caria F, et al. Neuromuscul Disord. 2019 Sep;29(9):657-663. doi: 10.1016/j.nmd.2019.07.007. Epub 2019 Jul 30. Neuromuscul Disord. 2019. PMID: 31471117
Two adult siblings presented with muscle weakness and wasting, elbows and Achilles tendon retractions, lumbar hyperlordosis, waddling gait and positive Gowers' sign. Muscle biopsy showed a dystrophic pattern. Molecular analysis of the COL6A2 gene revealed the novel …
Two adult siblings presented with muscle weakness and wasting, elbows and Achilles tendon retractions, lumbar hyperlordosis, waddling gait a …
Gowers' sign in children with discitis of the lumbar spine.
Mirovsky Y, Copeliovich L, Halperin N. Mirovsky Y, et al. J Pediatr Orthop B. 2005 Mar;14(2):68-70. doi: 10.1097/01202412-200503000-00002. J Pediatr Orthop B. 2005. PMID: 15703513
Gowers' sign is pathognomonic in patients with Duchenne muscular dystrophy. ...We report on four children in the age range of 3.3-8 years with disc space infection in the lumbar region, who demonstrated the sign in the early stages of the disease. Following treatmen …
Gowers' sign is pathognomonic in patients with Duchenne muscular dystrophy. ...We report on four children in the age range of …
Prednisolone in Duchenne muscular dystrophy with imminent loss of ambulation.
Pradhan S, Ghosh D, Srivastava NK, Kumar A, Mittal B, Pandey CM, Singh U. Pradhan S, et al. J Neurol. 2006 Oct;253(10):1309-16. doi: 10.1007/s00415-006-0212-1. Epub 2006 Jun 19. J Neurol. 2006. PMID: 16786214 Clinical Trial.
Till the ideal stage of the disease and the type or dosage of starting steroid therapy is defined by specially designed studies, 0.75 mg/Kg/day prednisolone therapy may be started in DMD patients at the stage of frequent falls ( > 10 / day) on walking or increased get-up time …
Till the ideal stage of the disease and the type or dosage of starting steroid therapy is defined by specially designed studies, 0.75 mg/Kg/ …
Turner Syndrome Mosaicism 45,X/46,XY with Genital Ambiguity and Duchenne Muscular Dystrophy: Translational Approach of a Rare Italian Case.
Lamanna B, Vinciguerra M, Dellino M, Cascella G, Cazzato G, Macorano E, Malvasi A, Scacco S, Cicinelli E, Loizzi V, Vimercati A, Cormio G, Paduano F, Cascardi E, Tatullo M. Lamanna B, et al. Int J Mol Sci. 2022 Nov 19;23(22):14408. doi: 10.3390/ijms232214408. Int J Mol Sci. 2022. PMID: 36430887 Free PMC article.
At the age of three years, she had increasing difficulty walking, running, jumping and climbing stairs, proximal upper and lower extremity muscle weakness and a positive Gowers' sign. In addition, the serum creatine kinase (CK) value was over 30X the upper limit of …
At the age of three years, she had increasing difficulty walking, running, jumping and climbing stairs, proximal upper and lower extremity m …
Corneal clouding: An infrequent ophthalmic manifestation of mitochondrial disease.
Lee HF, Lee HJ, Chi CS, Tsai CR, Chang P. Lee HF, et al. Pediatr Neurol. 2006 Jun;34(6):464-6. doi: 10.1016/j.pediatrneurol.2005.12.002. Pediatr Neurol. 2006. PMID: 16765825
Clinical conditions worsened, including ptosis, progressive weakness, and positive Gowers' sign. Oral glucose lactate stimulation test was positive, therefore a muscle biopsy was performed at 11 years of age. ...
Clinical conditions worsened, including ptosis, progressive weakness, and positive Gowers' sign. Oral glucose lactate stimulat …
Mental retardation in congenital nonprogressive myopathy with uniform type 1 fibers.
Jong YJ, Huang SC, Liu GC, Chiang CH. Jong YJ, et al. Brain Dev. 1991 Nov;13(6):444-6. doi: 10.1016/s0387-7604(12)80046-5. Brain Dev. 1991. PMID: 1810161
She had a myopathic face, high-arched palate, nasal tone vocalization, positive Gowers' sign, waddling gait and decreased deep tendon reflexes. Her IQ was 40 (PIQ = 39, VIQ = 51). ...
She had a myopathic face, high-arched palate, nasal tone vocalization, positive Gowers' sign, waddling gait and decreased deep …