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

Year Number of Results
1964 1
1965 1
1966 1
1967 8
1968 10
1969 2
1970 4
1971 8
1972 7
1973 2
1974 6
1975 1
1976 1
1977 1
1978 1
1979 1
1980 1
1981 1
1982 2
1983 2
1985 1
1987 1
1988 3
1989 2
1990 1
1991 2
1992 8
1993 3
1994 3
1995 2
1996 6
1997 2
1998 2
1999 3
2000 6
2001 4
2002 10
2003 13
2004 8
2005 11
2006 13
2007 6
2008 12
2009 7
2010 4
2011 7
2012 10
2013 16
2014 8
2015 12
2016 13
2017 6
2018 9
2019 13
2020 5
2021 6
2022 8
2023 8
2024 2

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297 results

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Page 1
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). ...Conversely, chron …
Genetic pain loss includes congenital insensitivity to pain (CIP), hereditary sensory neuropathies …
Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy.
Adams D, Ando Y, Beirão JM, Coelho T, Gertz MA, Gillmore JD, Hawkins PN, Lousada I, Suhr OB, Merlini G. Adams D, et al. J Neurol. 2021 Jun;268(6):2109-2122. doi: 10.1007/s00415-019-09688-0. Epub 2020 Jan 6. J Neurol. 2021. PMID: 31907599 Free PMC article. Review.
Amyloid transthyretin (ATTR) amyloidosis with polyneuropathy (PN) is a progressive, debilitating, systemic disease wherein transthyretin protein misfolds to form amyloid, which is deposited in the endoneurium. ATTR amyloidosis with PN is the most serious hereditary polyneu …
Amyloid transthyretin (ATTR) amyloidosis with polyneuropathy (PN) is a progressive, debilitating, systemic disease wherein transthyretin pro …
A Clinician's Approach to Peripheral Neuropathy.
Siao P, Kaku M. Siao P, et al. Semin Neurol. 2019 Oct;39(5):519-530. doi: 10.1055/s-0039-1694747. Epub 2019 Oct 22. Semin Neurol. 2019. PMID: 31639835 Review.
Peripheral neuropathies are a group of disorders that affect the peripheral nervous system, for which hundreds of etiologies have been identified. ...Such patterns include acute versus chronic, primary demyelinating versus axonal, hereditary versus acquired, asymmet …
Peripheral neuropathies are a group of disorders that affect the peripheral nervous system, for which hundreds of etiologies have bee …
Charcot-Marie-Tooth Disease and Other Hereditary Neuropathies.
Klein CJ. Klein CJ. Continuum (Minneap Minn). 2020 Oct;26(5):1224-1256. doi: 10.1212/CON.0000000000000927. Continuum (Minneap Minn). 2020. PMID: 33003000 Review.
PURPOSE OF REVIEW: This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These disorders encompass a broad spectrum with variable motor, sensory, autonomic, and other organ system involvement. ...Emerging the …
PURPOSE OF REVIEW: This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These dis …
Familial dysautonomia.
González-Duarte A, Cotrina-Vidal M, Kaufmann H, Norcliffe-Kaufmann L. González-Duarte A, et al. Clin Auton Res. 2023 Jun;33(3):269-280. doi: 10.1007/s10286-023-00941-1. Epub 2023 May 19. Clin Auton Res. 2023. PMID: 37204536 Review.
Familial dysautonomia (FD) is an autosomal recessive hereditary sensory and autonomic neuropathy (HSAN, type 3) expressed at birth with profound sensory loss and early death. ...Neurogenic dysphagia causes frequent aspiration leading to chronic pulmona …
Familial dysautonomia (FD) is an autosomal recessive hereditary sensory and autonomic neuropathy (HSAN, type 3) express …
Inherited Neuropathies.
Carroll AS, Burns J, Nicholson G, Kiernan MC, Vucic S. Carroll AS, et al. Semin Neurol. 2019 Oct;39(5):620-639. doi: 10.1055/s-0039-1693006. Epub 2019 Oct 22. Semin Neurol. 2019. PMID: 31639845 Review.
The inherited neuropathies are a common and heterogeneous group of slowly progressive disorders affecting motor, sensory, and autonomic nerves. These hereditary conditions can be confined to the peripheral nervous system, termed the primary heredita …
The inherited neuropathies are a common and heterogeneous group of slowly progressive disorders affecting motor, sensory, and …
Congenital Insensitivity to Pain: A Misnomer.
Weisman A, Quintner J, Masharawi Y. Weisman A, et al. J Pain. 2019 Sep;20(9):1011-1014. doi: 10.1016/j.jpain.2019.01.331. Epub 2019 Feb 2. J Pain. 2019. PMID: 30716471 Free article. Review.
Congenital insensitivity to pain is an umbrella term used to describe a group of rare genetic diseases also classified as hereditary sensory autonomic neuropathies. ...The suggested term better reflects the nature of the conditions and in …
Congenital insensitivity to pain is an umbrella term used to describe a group of rare genetic diseases also classified as h …
Hereditary neuropathies: An update.
Stojkovic T. Stojkovic T. Rev Neurol (Paris). 2016 Dec;172(12):775-778. doi: 10.1016/j.neurol.2016.06.007. Epub 2016 Nov 17. Rev Neurol (Paris). 2016. PMID: 27866730 Review.
Hereditary neuropathies are the most common inherited neuromuscular diseases. ...Moreover, atypical phenotypes are arising, overlapping with spastic paraplegia, hereditary sensory neuropathies or amyotrophic lateral sclerosis. The causative gene …
Hereditary neuropathies are the most common inherited neuromuscular diseases. ...Moreover, atypical phenotypes are arising, ov …
Autonomic neuropathies.
Low PA. Low PA. Curr Opin Neurol. 2002 Oct;15(5):605-9. doi: 10.1097/00019052-200210000-00011. Curr Opin Neurol. 2002. PMID: 12352004 Review.
Sympathetic cardiac hyperinnervation can occur concurrently with denervation in diabetic neuropathy The gene mutations for hereditary sensory and autonomic neuropathies I, III, and IV are now known and there is clear unmyelinated fiber loss. ... …
Sympathetic cardiac hyperinnervation can occur concurrently with denervation in diabetic neuropathy The gene mutations for hereditary …
Familial dysautonomia.
Axelrod FB. Axelrod FB. Muscle Nerve. 2004 Mar;29(3):352-63. doi: 10.1002/mus.10499. Muscle Nerve. 2004. PMID: 14981733 Review.
Familial dysautonomia (FD) is a neurodevelopmental genetic disorder within the larger classification of hereditary sensory and autonomic neuropathies, each caused by a different genetic error. ...Pathological alterations consist of decreased unm …
Familial dysautonomia (FD) is a neurodevelopmental genetic disorder within the larger classification of hereditary sensory …
297 results