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1981 1
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Page 1
Diabetic Lumbosacral Radiculoplexus Neuropathy (Diabetic Amyotrophy).
Glenn MD, Jabari D. Glenn MD, et al. Neurol Clin. 2020 Aug;38(3):553-564. doi: 10.1016/j.ncl.2020.03.010. Neurol Clin. 2020. PMID: 32703468 Review.
Diabetic lumbosacral radiculoplexus neuropathy, also known as diabetic amyotrophy, has a characteristic course of sudden onset of unilateral pain in the thigh and hip, which may spread to the other side in weeks to months and proceeds with progressive lower extre
Diabetic lumbosacral radiculoplexus neuropathy, also known as diabetic amyotrophy, has a characteristic course of sudden onset of uni …
Distal myopathy.
Savarese M, Jokela M, Udd B. Savarese M, et al. Handb Clin Neurol. 2023;195:497-519. doi: 10.1016/B978-0-323-98818-6.00002-9. Handb Clin Neurol. 2023. PMID: 37562883 Review.
Distal myopathies are a group of genetic, primary muscle diseases. Patients develop progressive weakness and atrophy of the muscles of forearm, hands, lower leg, or feet. ...This chapter provides a description of the clinicopathologic and genetic aspects of
Distal myopathies are a group of genetic, primary muscle diseases. Patients develop progressive weakness and atrophy of the mu
Cervical spondylotic amyotrophy.
Jiang SD, Jiang LS, Dai LY. Jiang SD, et al. Eur Spine J. 2011 Mar;20(3):351-7. doi: 10.1007/s00586-010-1544-1. Epub 2010 Aug 8. Eur Spine J. 2011. PMID: 20694735 Free PMC article. Review.
Cervical spondylotic amyotrophy is characterized with weakness and wasting of upper limb muscles without sensory or lower limb involvement. ...Cervical spondylotic amyotrophy is classified according to the most predominantly affected muscle grou …
Cervical spondylotic amyotrophy is characterized with weakness and wasting of upper limb muscles without sensory or lower
Perspectives of Kennedy's disease.
Finsterer J. Finsterer J. J Neurol Sci. 2010 Nov 15;298(1-2):1-10. doi: 10.1016/j.jns.2010.08.025. Epub 2010 Sep 16. J Neurol Sci. 2010. PMID: 20846673 Review.
Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare, adult-onset, X-linked, recessive trinucleotide, polyglutamine (poly-G) disorder, caused by expansion of an unstable CAG-tandem-repeat in exon 1 of the androgen-receptor (AR) gene on chr …
Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare, adult-onset, X-linked, recessive trinucleotid …
Atopy and neural damage.
Kira J. Kira J. Intern Med. 2002 Mar;41(3):169-74. doi: 10.2169/internalmedicine.41.169. Intern Med. 2002. PMID: 11929175 Free article. Review.
In addition, we also found that Hirayama disease, juvenile muscular atrophy of the distal upper extremity, is also associated with airway allergy such as allergic rhinitis and atopic asthma. ...Moreover, by the prospective study of the history of aller …
In addition, we also found that Hirayama disease, juvenile muscular atrophy of the distal upper extremity, is al …
Vascular anomalies and the growth of limbs: a review.
Enjolras O, Chapot R, Merland JJ. Enjolras O, et al. J Pediatr Orthop B. 2004 Nov;13(6):349-57. doi: 10.1097/01202412-200411000-00001. J Pediatr Orthop B. 2004. PMID: 15599224 Review.
Treatment is generally conservative. An affected lower extremity can be complicated by pelvic tilting and scoliosis because leg length discrepancy may reach 10 cm. To avoid such a course, stapling epiphysiodesis of the knee cartilages is often performed, but this or …
Treatment is generally conservative. An affected lower extremity can be complicated by pelvic tilting and scoliosis because le …
[Progress of clinical and genetic research on distal hereditary motor neuropathy].
Cao L, Zhao G. Cao L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1136-1140. doi: 10.3760/cma.j.issn.1003-9406.2019.11.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703145 Review. Chinese.
Distal hereditary motor neuropathy (dHMN) is a group of clinically and genetically heterogeneous disorders characterized by progressive distal weakness and atrophy. The onset of dHMN is at mid-adulthood or early childhood, and the symptoms are mainly present
Distal hereditary motor neuropathy (dHMN) is a group of clinically and genetically heterogeneous disorders characterized by progressi
Classification, differential diagnosis, and staging of diabetic peripheral neuropathy.
Thomas PK. Thomas PK. Diabetes. 1997 Sep;46 Suppl 2:S54-7. doi: 10.2337/diab.46.2.s54. Diabetes. 1997. PMID: 9285500 Review.
A distal axonopathy of dying-back type may represent the underlying pathogenetic basis. Other more persistent phenomena consist of focal and multifocal lesions giving rise to cranial, thoraco-abdominal, and limb neuropathies, including proximal lower limb
A distal axonopathy of dying-back type may represent the underlying pathogenetic basis. Other more persistent phenomena consist of fo …
SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome.
Horga A, Tomaselli PJ, Gonzalez MA, Laurà M, Muntoni F, Manzur AY, Hanna MG, Blake JC, Houlden H, Züchner S, Reilly MM. Horga A, et al. Neurology. 2016 Oct 11;87(15):1607-1612. doi: 10.1212/WNL.0000000000003212. Epub 2016 Sep 14. Neurology. 2016. PMID: 27629094 Free PMC article. Review.
OBJECTIVE: To describe the genetic and clinical features of a simplex patient with distal hereditary motor neuropathy (dHMN) and lower limb spasticity (Silver-like syndrome) due to a mutation in the sigma nonopioid intracellular receptor-1 gene (SIGMAR1) and …
OBJECTIVE: To describe the genetic and clinical features of a simplex patient with distal hereditary motor neuropathy (dHMN) and l
Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective.
Hassan KM, Sahni H. Hassan KM, et al. Biomed Res Int. 2013;2013:478516. doi: 10.1155/2013/478516. Epub 2013 Aug 26. Biomed Res Int. 2013. PMID: 24063005 Free PMC article. Review.
Since its original description by Keizo Hirayama in 1959, "juvenile muscular atrophy of the unilateral upper extremity" has been described under many nomenclatures from the east. ...HD presents in adolescence and young adulthood with insidious onset unilatera …
Since its original description by Keizo Hirayama in 1959, "juvenile muscular atrophy of the unilateral upper extremity" …
25 results