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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 and, i …
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.
Such patterns include acute versus chronic, primary demyelinating versus axonal, hereditary versus acquired, asymmetric versus symmetric, presence of facial palsies, sensory or motor predominant, and presence of prominent autonomic symptoms. ...Skin biopsy ma …
Such patterns include acute versus chronic, primary demyelinating versus axonal, hereditary versus acquired, asymmetric versus symmet …
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.
Symptoms may be mistakenly attributed to other diseases such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), idiopathic axonal polyneuropathy, lumbar spinal stenosis, and, more rarely, diabetic neuropathy and AL amyloidosis. In endemic countries (e.g., …
Symptoms may be mistakenly attributed to other diseases such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), idiopathic …
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. ...New therapie …
PURPOSE OF REVIEW: This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These dis …
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 …
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. ...Progressive features of the disease include retinal nerve fi …
Familial dysautonomia (FD) is an autosomal recessive hereditary sensory and autonomic neuropathy (HSAN, type 3) …
Inherited polyneuropathies.
Rinaldi R, Patel A. Rinaldi R, et al. PM R. 2013 May;5(5 Suppl):S63-73. doi: 10.1016/j.pmrj.2013.03.028. Epub 2013 Mar 28. PM R. 2013. PMID: 23542772 Review.
The large degree of clinical heterogeneity within each of the major categories of inherited neuropathies can lead to difficulties in making correct diagnoses based on clinical findings alone. ...
The large degree of clinical heterogeneity within each of the major categories of inherited neuropathies can lead to difficulties in …
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. ...An accurate genetic diagnosis is important for appropriate genetic counselling and treatment options. Therapeutic advances, particularly small interfering RNA therapy, are encour …
Hereditary neuropathies are the most common inherited neuromuscular diseases. ...An accurate genetic diagnosis is important fo …
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. ...Sensory loss includes impaired pain …
Familial dysautonomia (FD) is a neurodevelopmental genetic disorder within the larger classification of hereditary sensory …
Neuroimaging in Sensory Neuronopathy.
Casseb RF, Martinez AR, de Paiva JL, França MC Jr. Casseb RF, et al. J Neuroimaging. 2015 Sep-Oct;25(5):704-9. doi: 10.1111/jon.12210. Epub 2015 Feb 10. J Neuroimaging. 2015. PMID: 25678358 Review.
Sensory neuronopathies (SN) are a group of disorders characterized by primary damage to the dorsal root ganglia neurons. Clinical features include multifocal areas of hypoaesthesia, pain, dysautonomia, and sensory ataxia, which is the major source of disability. Dia …
Sensory neuronopathies (SN) are a group of disorders characterized by primary damage to the dorsal root ganglia neurons. Clinical fea …
297 results