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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1987 1
1988 3
1989 8
1990 5
1991 5
1992 5
1993 6
1994 4
1995 7
1996 7
1997 5
1998 7
1999 11
2000 8
2001 7
2002 7
2003 8
2004 9
2005 12
2006 13
2007 9
2008 22
2009 15
2010 11
2011 19
2012 18
2013 13
2014 13
2015 18
2016 21
2017 13
2018 19
2019 11
2020 12
2021 9
2022 12
2023 11
2024 6

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365 results

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Page 1
Differentiating lower motor neuron syndromes.
Garg N, Park SB, Vucic S, Yiannikas C, Spies J, Howells J, Huynh W, Matamala JM, Krishnan AV, Pollard JD, Cornblath DR, Reilly MM, Kiernan MC. Garg N, et al. J Neurol Neurosurg Psychiatry. 2017 Jun;88(6):474-483. doi: 10.1136/jnnp-2016-313526. Epub 2016 Dec 21. J Neurol Neurosurg Psychiatry. 2017. PMID: 28003344 Free PMC article. Review.
Lower motor neuron (LMN) syndromes typically present with muscle wasting and weakness and may arise from pathology affecting the distal motor nerve up to the level of the anterior horn cell. A variety of hereditary causes are recognised, including spinal musc …
Lower motor neuron (LMN) syndromes typically present with muscle wasting and weakness and may arise from pathology affecting t …
Mechanical ventilation and COPD: from pathophysiology to ventilatory management.
Scaramuzzo G, Ottaviani I, Volta CA, Spadaro S. Scaramuzzo G, et al. Minerva Med. 2022 Jun;113(3):460-470. doi: 10.23736/S0026-4806.22.07974-5. Minerva Med. 2022. PMID: 35856181 Free article. Review.
Lung emphysema and reduced elastic recoil increase expiratory time, thus worsening dynamic hyperinflation, while airways chronic inflammation rises resistances and can determine distal air-trapping. Muscle wasting and fast fibers prevalence can result in weakness
Lung emphysema and reduced elastic recoil increase expiratory time, thus worsening dynamic hyperinflation, while airways chronic inflammatio …
Chronic Inflammatory Demyelinating Polyneuropathy.
Kuwabara S, Misawa S. Kuwabara S, et al. Adv Exp Med Biol. 2019;1190:333-343. doi: 10.1007/978-981-32-9636-7_21. Adv Exp Med Biol. 2019. PMID: 31760654 Review.
Typical CIDP is a most common form, characterized by symmetric proximal and distal muscle weakness and motor-dominant manifestation. In typical CIDP, demyelination predominantly affects the distal nerve terminals and nerve roots, where the blood-nerve …
Typical CIDP is a most common form, characterized by symmetric proximal and distal muscle weakness and motor-dominant m …
The muscular dystrophies.
Emery AE. Emery AE. Lancet. 2002 Feb 23;359(9307):687-95. doi: 10.1016/S0140-6736(02)07815-7. Lancet. 2002. PMID: 11879882 Review.
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable distribution and severity. They can be subdivided into several groups, including congenital forms, in accordance with the distribution of p …
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable …
Post-polio syndrome and rehabilitation.
Tiffreau V, Rapin A, Serafi R, Percebois-Macadré L, Supper C, Jolly D, Boyer FC. Tiffreau V, et al. Ann Phys Rehabil Med. 2010 Feb;53(1):42-50. doi: 10.1016/j.rehab.2009.11.007. Epub 2009 Dec 30. Ann Phys Rehabil Med. 2010. PMID: 20044320 Free article. Review.
An overuse of enlarged motor units is suspected causing denervation again due to distal degeneration of axons. Metabolic and functional changes has been described in muscle fibers of partially denervated muscles. Nevertheless, submaximal aerobic training and low int …
An overuse of enlarged motor units is suspected causing denervation again due to distal degeneration of axons. Metabolic and function …
Panorama of the distal myopathies.
Savarese M, Sarparanta J, Vihola A, Jonson PH, Johari M, Rusanen S, Hackman P, Udd B. Savarese M, et al. Acta Myol. 2020 Dec 1;39(4):245-265. doi: 10.36185/2532-1900-028. eCollection 2020 Dec. Acta Myol. 2020. PMID: 33458580 Free PMC article. Review.
Distal myopathies are genetic primary muscle disorders with a prominent weakness at onset in hands and/or feet. The age of onset (from early childhood to adulthood), the distribution of muscle weakness (upper versus lower limbs) and the histolog
Distal myopathies are genetic primary muscle disorders with a prominent weakness at onset in hands and/or feet. The age
Juvenile Dermatomyositis: Advances in Pathogenesis, Assessment, and Management.
Leung AKC, Lam JM, Alobaida S, Leong KF, Wong AHC. Leung AKC, et al. Curr Pediatr Rev. 2021;17(4):273-287. doi: 10.2174/1573396317666210426105045. Curr Pediatr Rev. 2021. PMID: 33902423 Review.
In 2017, the European League Against Rheumatism (EULAR) and the American College of Rheumatology (ACR) developed diagnostic criteria for juvenile idiopathic inflammatory myopathies and juvenile dermatomyositis. In the absence of muscle biopsies which are infrequently perfo …
In 2017, the European League Against Rheumatism (EULAR) and the American College of Rheumatology (ACR) developed diagnostic criteria for juv …
Collagen VI in the Musculoskeletal System.
Di Martino A, Cescon M, D'Agostino C, Schilardi F, Sabatelli P, Merlini L, Faldini C. Di Martino A, et al. Int J Mol Sci. 2023 Mar 7;24(6):5095. doi: 10.3390/ijms24065095. Int J Mol Sci. 2023. PMID: 36982167 Free PMC article. Review.
Mutations in the genes encoding collagen VI main chains, COL6A1, COL6A2 and COL6A3, are responsible for a spectrum of congenital muscular disorders, namely Ullrich congenital muscular dystrophy (UCMD), Bethlem myopathy (BM) and myosclerosis myopathy (MM), which show a variable co …
Mutations in the genes encoding collagen VI main chains, COL6A1, COL6A2 and COL6A3, are responsible for a spectrum of congenital muscular di …
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 extremity weakness
Diabetic lumbosacral radiculoplexus neuropathy, also known as diabetic amyotrophy, has a characteristic course of sudden onset of unilateral …
Chronic inflammatory demyelinating polyneuropathy: update on diagnosis, immunopathogenesis and treatment.
Lehmann HC, Burke D, Kuwabara S. Lehmann HC, et al. J Neurol Neurosurg Psychiatry. 2019 Sep;90(9):981-987. doi: 10.1136/jnnp-2019-320314. Epub 2019 Apr 16. J Neurol Neurosurg Psychiatry. 2019. PMID: 30992333 Review.
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an immune-mediated neuropathy typically characterised by symmetrical involvement, and proximal as well as distal muscle weakness (typical CIDP). However, there are several 'atypical' subtypes, such a …
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an immune-mediated neuropathy typically characterised by symmetrical involvement …
365 results