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

Year Number of Results
1964 1
1967 2
1968 6
1969 4
1970 3
1971 8
1972 2
1973 1
1974 5
1975 4
1977 1
1978 3
1979 1
1980 2
1981 1
1982 1
1983 4
1984 5
1985 1
1986 2
1987 4
1988 8
1989 2
1990 6
1991 8
1992 9
1993 9
1994 7
1995 8
1996 6
1997 7
1998 15
1999 15
2000 21
2001 7
2002 10
2003 12
2004 9
2005 11
2006 14
2007 11
2008 16
2009 13
2010 12
2011 15
2012 16
2013 14
2014 21
2015 26
2016 30
2017 30
2018 32
2019 31
2020 18
2021 19
2022 18
2023 11
2024 5

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Search Results

525 results

Results by year

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Page 1
Neonatal hypotonia and neuromuscular conditions.
Mercuri E, Pera MC, Brogna C. Mercuri E, et al. Handb Clin Neurol. 2019;162:435-448. doi: 10.1016/B978-0-444-64029-1.00021-7. Handb Clin Neurol. 2019. PMID: 31324324 Review.
The differential diagnosis of neonatal hypotonia is a complex task, as in newborns hypotonia can be the presenting sign of different underlying causes, including peripheral and central nervous system involvement and genetic and metabolic diseases. This …
The differential diagnosis of neonatal hypotonia is a complex task, as in newborns hypotonia can be the presenting sign of different underly …
Genetic pain loss disorders.
Lischka A, Lassuthova P, Çakar A, Record CJ, Van Lent J, Baets J, Dohrn MF, Senderek J, Lampert A, Bennett DL, Wood JN, Timmerman V, Hornemann T, Auer-Grumbach M, Parman Y, Hübner CA, Elbracht M, Eggermann K, Geoffrey Woods C, Cox JJ, Reilly MM, Kurth I. Lischka A, et al. Nat Rev Dis Primers. 2022 Jun 16;8(1):41. doi: 10.1038/s41572-022-00365-7. Nat Rev Dis Primers. 2022. PMID: 35710757 Review.
Genetic pain loss includes congenital insensitivity to pain (CIP), hereditary sensory neuropathies and, if autonomic nerves are involved, hereditary sensory and autonomic neuropathy (HSAN). ...Given the progress that has been made, the coming years are promising bot …
Genetic pain loss includes congenital insensitivity to pain (CIP), hereditary sensory neuropathies and, if autonomic nerves are invol …
Thoracic outlet syndrome: a review.
Panther EJ, Reintgen CD, Cueto RJ, Hao KA, Chim H, King JJ. Panther EJ, et al. J Shoulder Elbow Surg. 2022 Nov;31(11):e545-e561. doi: 10.1016/j.jse.2022.06.026. Epub 2022 Aug 10. J Shoulder Elbow Surg. 2022. PMID: 35963513 Review.
TOS can be classified as neurogenic, arterial, or venous based on the compressed structure(s). Patients develop TOS secondary to congenital abnormalities such as cervical ribs or fibrous bands originating from a cervical rib leading to an objectively verifiable form of TOS …
TOS can be classified as neurogenic, arterial, or venous based on the compressed structure(s). Patients develop TOS secondary to congenit …
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Ashrafi MR, Amanat M, Garshasbi M, Kameli R, Nilipour Y, Heidari M, Rezaei Z, Tavasoli AR. Ashrafi MR, et al. Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12. Expert Rev Neurother. 2020. PMID: 31829048 Review.
Introduction: Leukodystrophies constitute heterogenous group of rare heritable disorders primarily affecting the white matter of central nervous system. These conditions are often under-appreciated among physicians. ...New genetic methods and stem cell transplantati …
Introduction: Leukodystrophies constitute heterogenous group of rare heritable disorders primarily affecting the white matter of central …
Overview of Metatarsalgia.
Charen DA, Markowitz JS, Cheung ZB, Matijakovich DJ, Chan JJ, Vulcano E. Charen DA, et al. Orthopedics. 2019 Jan 1;42(1):e138-e143. doi: 10.3928/01477447-20181206-06. Epub 2018 Dec 13. Orthopedics. 2019. PMID: 30540873 Review.
Disorders of the enteric nervous system - a holistic view.
Niesler B, Kuerten S, Demir IE, Schäfer KH. Niesler B, et al. Nat Rev Gastroenterol Hepatol. 2021 Jun;18(6):393-410. doi: 10.1038/s41575-020-00385-2. Epub 2021 Jan 29. Nat Rev Gastroenterol Hepatol. 2021. PMID: 33514916 Review.
The enteric nervous system (ENS) is the largest division of the peripheral nervous system and closely resembles components and functions of the central nervous system. Although the central role of the ENS in congenital enter …
The enteric nervous system (ENS) is the largest division of the peripheral nervous system and closely res …
Walking and weakness in children: a narrative review of gait and functional ambulation in paediatric neuromuscular disease.
Kennedy RA, Carroll K, McGinley JL, Paterson KL. Kennedy RA, et al. J Foot Ankle Res. 2020 Mar 2;13(1):10. doi: 10.1186/s13047-020-0378-2. J Foot Ankle Res. 2020. PMID: 32122377 Free PMC article. Review.
BACKGROUND: Weakness is the primary impairment in paediatric neuromuscular diseases, impacting gait and gait-related functional activities in ambulant children affected by these rare and often degenerative diseases. ...The six-minute walk test is used widely as a te …
BACKGROUND: Weakness is the primary impairment in paediatric neuromuscular diseases, impacting gait and gait-related functional activ …
Dichloroacetate-induced peripheral neuropathy.
Stacpoole PW, Martyniuk CJ, James MO, Calcutt NA. Stacpoole PW, et al. Int Rev Neurobiol. 2019;145:211-238. doi: 10.1016/bs.irn.2019.05.003. Epub 2019 Jun 11. Int Rev Neurobiol. 2019. PMID: 31208525 Review.
By blocking PDK, DCA activates PDC and, consequently, the mitochondrial respiratory chain and ATP synthesis. A reversible sensory/motor peripheral neuropathy is the clinically limiting adverse effect of chronic DCA exposure and experimental data implicate the Schwan …
By blocking PDK, DCA activates PDC and, consequently, the mitochondrial respiratory chain and ATP synthesis. A reversible sensory/motor p …
Ciliopathy: Alström Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:179-180. doi: 10.1007/978-3-319-95046-4_35. Adv Exp Med Biol. 2018. PMID: 30578508 Review.
Patients present in childhood with photophobia and nystagmus, and mimic Leber congenital amaurosis (LCA). The fundus shows pigmentary retinopathy with peau d'orange appearance and some fine white dots like drusen around the macula; the disc is pale, with attenuated retinal …
Patients present in childhood with photophobia and nystagmus, and mimic Leber congenital amaurosis (LCA). The fundus shows pigmentary …
Hereditary sensory and autosomal peripheral neuropathy-type IV: case series and review of literature.
Ashwin DP, Chandan GD, Jasleen HK, Rajkumar GC, Rudresh KB, Prashanth R. Ashwin DP, et al. Oral Maxillofac Surg. 2015 Jun;19(2):117-23. doi: 10.1007/s10006-015-0486-5. Epub 2015 Mar 6. Oral Maxillofac Surg. 2015. PMID: 25744033 Review.
Hereditary sensory and autonomic neuropathy (HSAN) IV is a rare autosomal recessive disorder which is characterized by a decrease in the number of myelinated and non-myelinated nerve fibers of peripheral nerves which causes diminished or absent pain sensation leadin …
Hereditary sensory and autonomic neuropathy (HSAN) IV is a rare autosomal recessive disorder which is characterized by a decrease in …
525 results