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congenial sensory neuropathy相关文献:
Congenital sensory neuropathy with anhidrosis.
Ishii N, Kawaguchi H, Miyakawa K, Nakajima H.
Arch Dermatol. 1988 Apr;124(4):564-6.
PMID:3281596
Congenital sensory neuropathy. Ophthalmological implications.
Pinckers A, van 't Pad Bosch AA, Aandekerk AL, Cruysberg JR.
Acta Ophthalmol (Copenh). 1988 Jun;66(3):293-8. doi: 10.1111/j.1755-3768.1988.tb04599.x.
PMID:10994450
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.
Nat Rev Dis Primers. 2022 Jun 16;8(1):41. doi: 10.1038/s41572-022-00365-7.
PMID:35710757
Hereditary sensory neuropathies.
Houlden H, Blake J, Reilly MM.
Curr Opin Neurol. 2004 Oct;17(5):569-77. doi: 10.1097/00019052-200410000-00007.
PMID:15367861
Congenital sensory neuropathy with skeletal dysplasia.
Axelrod FB, Pearson J, Tepperberg J, Ackerman BD.
J Pediatr. 1983 May;102(5):727-30. doi: 10.1016/s0022-3476(83)80246-7.
PMID:6573468
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort.
Cintra VP, Dohrn MF, Tomaselli PJ, Figueiredo FB, Marques SE, Camargos ST, Barbosa LSM, P Rebelo A, Abreu L, Danzi M, Marques W Jr, Züchner S.
J Neurol Sci. 2021 Aug 15;427:117498. doi: 10.1016/j.jns.2021.117498. Epub 2021 May 18.
PMID:34090020
Congenital sensory neuropathy.
WADIA NH, DASTUR DK.
World Neurol. 1960 Nov;1:409-21.
PMID:13782423
Congenital sensory neuropathy.
Schneiderman MJ.
Am J Dis Child. 1986 Nov;140(11):1100. doi: 10.1001/archpedi.1986.02140250026023.
PMID:3464198
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV).
Rosemberg S, Marie SK, Kliemann S.
Pediatr Neurol. 1994 Jul;11(1):50-6. doi: 10.1016/0887-8994(94)90091-4.
PMID:7527213
Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
Indo Y.
Clin Auton Res. 2002 May;12 Suppl 1:I20-32. doi: 10.1007/s102860200016.
PMID:12102460
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