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Quoted phrase not found in phrase index: "Degeneration of anterior horn cells"
Page 1
Multiple congenital contractures.
Vanpaemel L, Schoenmakers M, van Nesselrooij B, Pruijs H, Helders P. Vanpaemel L, et al. J Pediatr Orthop B. 1997 Jul;6(3):172-8. doi: 10.1097/01202412-199707000-00004. J Pediatr Orthop B. 1997. PMID: 9260645
All treatments that patients received so far as well as functional outcome were studied. We compared these factors in children with anterior horn cell degeneration (AHCD) or amyoplasia with those of children with contractures of other origin. ...
All treatments that patients received so far as well as functional outcome were studied. We compared these factors in children with anter …
Pregnancy outcomes in women with spinal muscular atrophy: A review.
Abati E, Corti S. Abati E, et al. J Neurol Sci. 2018 May 15;388:50-60. doi: 10.1016/j.jns.2018.03.001. Epub 2018 Mar 2. J Neurol Sci. 2018. PMID: 29627031 Review.
Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by muscle weakness and atrophy resulting from progressive degeneration and loss of the anterior horn cells in the spinal cord and brain stem nuclei. ...
Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by muscle weakness and atrophy resulting from progressive d …
Drug treatment for spinal muscular atrophy type I.
Wadman RI, Bosboom WM, van der Pol WL, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Wadman RI, et al. Cochrane Database Syst Rev. 2012 Apr 18;(4):CD006281. doi: 10.1002/14651858.CD006281.pub4. Cochrane Database Syst Rev. 2012. Update in: Cochrane Database Syst Rev. 2019 Dec 11;12:CD006281. doi: 10.1002/14651858.CD006281.pub5. PMID: 22513939 Updated. Review.
BACKGROUND: Spinal muscular atrophy (SMA) is caused by degeneration of anterior horn cells of the spinal cord, which leads to progressive muscle weakness. ...
BACKGROUND: Spinal muscular atrophy (SMA) is caused by degeneration of anterior horn cells of the spinal cord, w …
Drug treatment for spinal muscular atrophy type I.
Bosboom W, Vrancken AF, van den Berg LH, Wokke J, Iannaccone ST. Bosboom W, et al. Cochrane Database Syst Rev. 2009 Jan 21;(1):CD006281. doi: 10.1002/14651858.CD006281.pub2. Cochrane Database Syst Rev. 2009. Update in: Cochrane Database Syst Rev. 2011 Dec 07;(12):CD006281. doi: 10.1002/14651858.CD006281.pub3. PMID: 19160274 Updated. Review.
BACKGROUND: Spinal muscular atrophy (SMA) is caused by degeneration of anterior horn cells, which leads to progressive muscle weakness. ...
BACKGROUND: Spinal muscular atrophy (SMA) is caused by degeneration of anterior horn cells, which leads to progr …
Presentation and Management Patterns of Lower Urinary Tract Symptoms in Adults Due to Rare Inherited Neuromuscular Diseases.
Roth JD, Pariser JJ, Stout TE, Misseri R, Elliott SP. Roth JD, et al. Urology. 2020 Jan;135:165-170. doi: 10.1016/j.urology.2019.09.039. Epub 2019 Oct 15. Urology. 2020. PMID: 31626855 Review.
Spinal muscular atrophy (n = 6) is a rare autosomal recessive disease characterized by degeneration of the anterior horn cells in the spinal cord and motor nuclei in the lower brainstem leading to progressive muscle weakness and atrophy. ...
Spinal muscular atrophy (n = 6) is a rare autosomal recessive disease characterized by degeneration of the anterior horn …
Spinal muscular atrophies: recent insights and impact on molecular diagnosis.
Brahe C, Bertini E. Brahe C, et al. J Mol Med (Berl). 1996 Oct;74(10):555-62. doi: 10.1007/s001090050059. J Mol Med (Berl). 1996. PMID: 8912176 Review.
Spinal muscular atrophies (SMA) are a group of motor neuron diseases characterized by degeneration of anterior horn cells of the spinal cord and by muscular atrophy. ...
Spinal muscular atrophies (SMA) are a group of motor neuron diseases characterized by degeneration of anterior horn …
Disorders of the motor neurone.
Morrison KE, Harding AE. Morrison KE, et al. Baillieres Clin Neurol. 1994 Aug;3(2):431-45. Baillieres Clin Neurol. 1994. PMID: 7952856 Review.
The spinal muscular atrophies (SMAs) are defined as a group of inherited disorders sharing the common pathological feature of degeneration of the anterior horn cells of the spinal cord and, in some cases, additionally of the bulbar motor nuclei. ...
The spinal muscular atrophies (SMAs) are defined as a group of inherited disorders sharing the common pathological feature of degeneratio …
The critical role of Hedgehog-responsive mesenchymal progenitors in meniscus development and injury repair.
Wei Y, Sun H, Gui T, Yao L, Zhong L, Yu W, Heo SJ, Han L, Dyment NA, Liu XS, Zhang Y, Koyama E, Long F, Zgonis MH, Mauck RL, Ahn J, Qin L. Wei Y, et al. Elife. 2021 Jun 4;10:e62917. doi: 10.7554/eLife.62917. Elife. 2021. PMID: 34085927 Free PMC article.
In culture, meniscal Gli1(+) cells possessed high progenitor activities under the control of Hh signal. Meniscus injury at the anterior horn induced a quick expansion of Gli1-lineage cells. Normally, meniscal tissue healed slowly, leading to cartilage …
In culture, meniscal Gli1(+) cells possessed high progenitor activities under the control of Hh signal. Meniscus injury at the ant …
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.
Tada M, Yokoseki A, Sato T, Makifuchi T, Onodera O. Tada M, et al. Adv Exp Med Biol. 2010;685:21-33. doi: 10.1007/978-1-4419-6448-9_3. Adv Exp Med Biol. 2010. PMID: 20687492 Review.
Neuropathological examination reveals severe loss of Purkinje cells and moderate neuronal loss in the anterior horn and dorsal root ganglia. ...APTX interacts with X-ray repair cross-complementing group 1 protein, which is a scaffold protein in SSBR. In addit …
Neuropathological examination reveals severe loss of Purkinje cells and moderate neuronal loss in the anterior horn and …
Drug treatment for spinal muscular atrophy types II and III.
Wadman RI, van der Pol WL, Bosboom WM, Asselman FL, van den Berg LH, Iannaccone ST, Vrancken AF. Wadman RI, et al. Cochrane Database Syst Rev. 2020 Jan 6;1(1):CD006282. doi: 10.1002/14651858.CD006282.pub5. Cochrane Database Syst Rev. 2020. PMID: 32006461 Free PMC article.
BACKGROUND: Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or a heterozygous deletion in combination with a (point) mutation in the second SMN1 allele. This results in degeneration of anterior …
BACKGROUND: Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron 1 (SMN1) gene on chromosome 5, or …
73 results