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Quoted phrase not found in phrase index: "Neuropathy, Recurrent, with Pressure Palsies"
Page 1
Inherited neuropathies.
Chance PF, Reilly M. Chance PF, et al. Curr Opin Neurol. 1994 Oct;7(5):372-80. doi: 10.1097/00019052-199410000-00002. Curr Opin Neurol. 1994. PMID: 7804455 Review.
CMTX is associated with mutations in the connexin 32 gene. CMT2 is an axonal neuropathy of undetermined cause. One form of CMT2 maps to chromosome 1p36 (CMT2A). Dejerine-Sottas disease is a severe, infantile-onset demyelinating polyneuropathy that may be associated with po …
CMTX is associated with mutations in the connexin 32 gene. CMT2 is an axonal neuropathy of undetermined cause. One form of CMT2 maps …
Hereditary neuralgic amyotrophy.
Meuleman J, Timmerman V, Van Broeckhoven C, De Jonghe P. Meuleman J, et al. Neurogenetics. 2001 Jul;3(3):115-8. doi: 10.1007/s100480100109. Neurogenetics. 2001. PMID: 11523561 Review.
Hereditary neuralgic amyotrophy (HNA) belongs to the group of recurrent focal neuropathies, the other major representative being hereditary neuropathy with liability to pressure palsies. ...Detailed analysis of these unlinked families has broade …
Hereditary neuralgic amyotrophy (HNA) belongs to the group of recurrent focal neuropathies, the other major representative bei …
Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy.
Topakian R, Wimmer S, Pischinger B, Pichler R. Topakian R, et al. BMJ Case Rep. 2014 Oct 17;2014:bcr2014206883. doi: 10.1136/bcr-2014-206883. BMJ Case Rep. 2014. PMID: 25326571 Free PMC article.
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal-dominant disorder associated with recurrent mononeuropathies following compression or trivial trauma. Reports on sciatic neuropathy as the presenting manifestation o …
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal-dominant disorder associated with re …
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom.
Karklinsky S, Kugler S, Bar-Yosef O, Nissenkorn A, Grossman-Jonish A, Tirosh I, Vivante A, Pode-Shakked B. Karklinsky S, et al. Ital J Pediatr. 2022 Jun 3;48(1):84. doi: 10.1186/s13052-022-01280-z. Ital J Pediatr. 2022. PMID: 35658923 Free PMC article.
BACKGROUND: Limping and/or refusal to walk is a common complaint in the setting of the pediatric department, with a widely diverse differential diagnosis. An unusual etiology, is that of a hereditary neuropathy. Hereditary neuropathy with liability to pressure …
BACKGROUND: Limping and/or refusal to walk is a common complaint in the setting of the pediatric department, with a widely diverse different …
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.
van Paassen BW, van der Kooi AJ, van Spaendonck-Zwarts KY, Verhamme C, Baas F, de Visser M. van Paassen BW, et al. Orphanet J Rare Dis. 2014 Mar 19;9:38. doi: 10.1186/1750-1172-9-38. Orphanet J Rare Dis. 2014. PMID: 24646194 Free PMC article. Review.
PMP22 related neuropathies comprise (1) PMP22 duplications leading to Charcot-Marie-Tooth disease type 1A (CMT1A), (2) PMP22 deletions, leading to Hereditary Neuropathy with liability to Pressure Palsies (HNPP), and (3) PMP22 point mutations, causing b …
PMP22 related neuropathies comprise (1) PMP22 duplications leading to Charcot-Marie-Tooth disease type 1A (CMT1A), (2) PMP22 deletion …
Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
Chance PF. Chance PF. Neuromolecular Med. 2006;8(1-2):159-74. doi: 10.1385/NMM:8:1:159. Neuromolecular Med. 2006. PMID: 16775374 Review.
Hereditary neuropathy with liability to pressure palsies (HNPP; also called tomaculous neuropathy) is an autosomal-dominant disorder that produces a painless episodic, recurrent, focal demyelinating neuropathy. ...Hereditary neuralgic amy …
Hereditary neuropathy with liability to pressure palsies (HNPP; also called tomaculous neuropathy) is an autosom …
Multiple tendon transfer for a case of radial nerve palsy in hereditary neuropathy with liability to pressure palsy.
Palumbo F, Yamamoto M, Hirata H. Palumbo F, et al. Nagoya J Med Sci. 2023 Feb;85(1):204-210. doi: 10.18999/nagjms.85.1.204. Nagoya J Med Sci. 2023. PMID: 36923620 Free PMC article. Review.
Hereditary neuropathy with liability to pressure palsy (HNPP) is a rare autosomal dominant disease characterized by focal, recurrent, demyelinating peripheral neuropathies. ...There is no standard surgical or pharmacological treatment. The course …
Hereditary neuropathy with liability to pressure palsy (HNPP) is a rare autosomal dominant disease characterized by focal, …
Hereditary neuropathy with liability to pressure palsies and amyotrophic lateral sclerosis.
Bhatt A, Farooq MU, Aburashed R, Kassab MY, Majid A, Bhatt S, Naravetla B, Dhaliwal G. Bhatt A, et al. Neurol Sci. 2009 Jun;30(3):241-5. doi: 10.1007/s10072-009-0034-x. Epub 2009 Feb 24. Neurol Sci. 2009. PMID: 19238316
A 56-year-old male with recurrent painless focal neuropathies and a family history of peripheral neuropathy of unknown etiology presented with progressively worsening of impaired sensations and weakness in his lower extremities. ...The patient was found to ha …
A 56-year-old male with recurrent painless focal neuropathies and a family history of peripheral neuropathy of unknown …
Shoulder dystocia: the unpreventable obstetric emergency with empiric management guidelines.
Gherman RB, Chauhan S, Ouzounian JG, Lerner H, Gonik B, Goodwin TM. Gherman RB, et al. Am J Obstet Gynecol. 2006 Sep;195(3):657-72. doi: 10.1016/j.ajog.2005.09.007. Epub 2006 Apr 21. Am J Obstet Gynecol. 2006. PMID: 16949396 Review.
In an evidence-based format, we sought to answer the following questions: (1) Is shoulder dystocia predictable? (2) Can shoulder dystocia be prevented? (3) When shoulder dystocia does occur, what maneuvers should be performed? ...From a prospective point of view, however, …
In an evidence-based format, we sought to answer the following questions: (1) Is shoulder dystocia predictable? (2) Can shoulder dyst …
Diagnosis of hereditary neuropathies in adult patients.
Pareyson D. Pareyson D. J Neurol. 2003 Feb;250(2):148-60. doi: 10.1007/s00415-003-1030-3. J Neurol. 2003. PMID: 12574944 Review.
Different phenotypes may be identified according to: disease course; involvement of motor, sensory, autonomic fibres; site of lesion (neuropathy versus neuronopathy); calibre of involved fibres (small-fibre versus large-fibre neuropathy); presence of distinct …
Different phenotypes may be identified according to: disease course; involvement of motor, sensory, autonomic fibres; site of lesion …
21 results