187 related articles for article (PubMed ID: 28471035)
21. Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report.
Singla S; Marwah N; Dutta S
J Dent Child (Chic); 2008; 75(2):207-11. PubMed ID: 18647521
[TBL] [Abstract][Full Text] [Related]
22. [Congenital insensitivity to pain, anhidrosis and premature loss of baby teeth as a symptoms of rare neuropathy].
Ahmed M; Hietala M; Huoponen K; Juntunen M; Jääskeläinen S; Penttinen M; Syrjänen S; Karjalainen S
Duodecim; 2005; 121(13):1429-32. PubMed ID: 16134716
[No Abstract] [Full Text] [Related]
23. Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia.
Zhao M; Chen YJ; Wang MW; Lin XH; Dong EL; Chen WJ; Wang N; Lin X
Mol Diagn Ther; 2019 Dec; 23(6):781-789. PubMed ID: 31630374
[TBL] [Abstract][Full Text] [Related]
24. Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia.
Daoud H; Papadima EM; Ouled Amar Bencheikh B; Katsila T; Dionne-Laporte A; Spiegelman D; Dion PA; Patrinos GP; Orrù S; Rouleau GA
Eur J Med Genet; 2015 Nov; 58(11):573-7. PubMed ID: 26260707
[TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 7527213
[TBL] [Abstract][Full Text] [Related]
26. Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegia.
Willkomm L; Heredia R; Hoffmann K; Wang H; Voit T; Hoffman EP; Cirak S
J Hum Genet; 2016 Jun; 61(6):571-3. PubMed ID: 26888483
[TBL] [Abstract][Full Text] [Related]
27. A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy.
Miyabayashi T; Ochiai T; Suzuki N; Aoki M; Inui T; Okubo Y; Sato R; Togashi N; Takashima H; Ishiura H; Tsuji S; Koh K; Takiyama Y; Haginoya K
J Hum Genet; 2019 Feb; 64(2):171-176. PubMed ID: 30467354
[TBL] [Abstract][Full Text] [Related]
28. Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.
Lu X; Cen Z; Xie F; Ouyang Z; Zhang B; Zhao G; Luo W
J Neurol Sci; 2014 Dec; 347(1-2):368-71. PubMed ID: 25454648
[TBL] [Abstract][Full Text] [Related]
29. A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.
Yu W; Jin H; Deng J; Nan D; Huang Y
BMC Med Genet; 2020 Jun; 21(1):123. PubMed ID: 32493220
[TBL] [Abstract][Full Text] [Related]
30. Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation.
Khan TN; Klar J; Tariq M; Anjum Baig S; Malik NA; Yousaf R; Baig SM; Dahl N
Eur J Hum Genet; 2014 Oct; 22(10):1180-4. PubMed ID: 24473461
[TBL] [Abstract][Full Text] [Related]
31. Non-truncating LIFR mutation: causal for prominent congenital pain insensitivity phenotype with progressive vertebral destruction?
Elsaid MF; Chalhoub N; Kamel H; Ehlayel M; Ibrahim N; Elsaid A; Kumar P; Khalak H; Ilyin VA; Suhre K; Abdel Aleem A
Clin Genet; 2016 Feb; 89(2):210-6. PubMed ID: 26285796
[TBL] [Abstract][Full Text] [Related]
32. From genes to pain: nerve growth factor and hereditary sensory and autonomic neuropathy type V.
Capsoni S
Eur J Neurosci; 2014 Feb; 39(3):392-400. PubMed ID: 24494679
[TBL] [Abstract][Full Text] [Related]
33. Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis.
Lee ST; Lee J; Lee M; Kim JW; Ki CS
Muscle Nerve; 2009 Nov; 40(5):855-9. PubMed ID: 19618435
[TBL] [Abstract][Full Text] [Related]
34. Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis.
Lin YP; Su YN; Weng WC; Lee WT
J Child Neurol; 2010 Dec; 25(12):1548-51. PubMed ID: 20647579
[TBL] [Abstract][Full Text] [Related]
35. 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
Oral Maxillofac Surg; 2015 Jun; 19(2):117-23. PubMed ID: 25744033
[TBL] [Abstract][Full Text] [Related]
36. Hereditary sensory neuropathy with spastic paraplegia.
Kherbaoui-Redouani L; Ploton D; Abely M; Bednarek N; Stourbe A; Sabouraud P; Motte J
Eur J Paediatr Neurol; 2004; 8(2):95-9. PubMed ID: 15253057
[TBL] [Abstract][Full Text] [Related]
37. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.
Houlden H; King RH; Hashemi-Nejad A; Wood NW; Mathias CJ; Reilly M; Thomas PK
Ann Neurol; 2001 Apr; 49(4):521-5. PubMed ID: 11310631
[TBL] [Abstract][Full Text] [Related]
38. TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability.
Heimer G; Oz-Levi D; Eyal E; Edvardson S; Nissenkorn A; Ruzzo EK; Szeinberg A; Maayan C; Mai-Zahav M; Efrati O; Pras E; Reznik-Wolf H; Lancet D; Goldstein DB; Anikster Y; Shalev SA; Elpeleg O; Ben Zeev B
Eur J Paediatr Neurol; 2016 Jan; 20(1):69-79. PubMed ID: 26542466
[TBL] [Abstract][Full Text] [Related]
39. Congenital insensitivity to pain with anhydrosis: report of a family case.
Labib S; Adnane Berdai M; Abourazzak S; Hida M; Harandou M
Pan Afr Med J; 2011; 9():33. PubMed ID: 22355435
[TBL] [Abstract][Full Text] [Related]
40. Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.
Moss C; Srinivas SM; Sarveswaran N; Nahorski M; Gowda VK; Browne FM; Woods G
Br J Dermatol; 2018 Nov; 179(5):1135-1140. PubMed ID: 29949203
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]