PubMed

Charcot-Marie-Tooth 1A concurrent with schwannomas of the spinal cord and median nerve.

Kwon JY, Chung KW, Park EK, Park SW, Choi BO.

J Korean Med Sci. 2009 Aug;24(4):763-6. Epub 2009 Jul 30.PMID: 19654968 [PubMed - indexed for MEDLINE]Related articlesFree article

Screening of the 17p11.2--p12 region in a large cohort of patients with Charcot-Marie-Tooth (CMT) disease or hereditary neuropathy with liability to pressure palsies (HNPP).

Kabzinska D, Pierscinska J, Kochanski A.

J Appl Genet. 2009;50(3):283-8.PMID: 19638685 [PubMed - indexed for MEDLINE]Related articlesFree article

PMP22 expression in dermal nerve myelin from patients with CMT1A.

Katona I, Wu X, Feely SM, Sottile S, Siskind CE, Miller LJ, Shy ME, Li J.

Brain. 2009 Jul;132(Pt 7):1734-40. Epub 2009 May 15.PMID: 19447823 [PubMed - indexed for MEDLINE]Related articles

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.

Neurol Sci. 2009 Jun;30(3):241-5. Epub 2009 Feb 24.PMID: 19238316 [PubMed - indexed for MEDLINE]Related articles

Hereditary neuropathy with liability to pressure palsy in childhood.

György I, Bíró A, Mechler F, Molnár MJ.

Ideggyogy Sz. 2008 Nov 30;61(11-12):423-5.PMID: 19070319 [PubMed - indexed for MEDLINE]Related articles

Late onset autosomal dominant Charcot-Marie-Tooth 2 neuropathy in a Costa Rican family.

Berghoff C, Berghoff M, Leal A, Morera B, Contreras C, Barrantes R, Rautenstrauss B, Del Valle G, Heuss D.

Neurol Res. 2009 Apr;31(3):283-8. Epub 2008 Sep 29.PMID: 18826755 [PubMed - indexed for MEDLINE]Related articles

Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype.

Al-Thihli K, Rudkin T, Carson N, Poulin C, Melançon S, Der Kaloustian VM.

Am J Med Genet A. 2008 Sep 15;146A(18):2412-6.PMID: 18698610 [PubMed - indexed for MEDLINE]Related articles

A new MPZ mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compression.

Magot A, Latour P, Mussini JM, Mourtada R, Guiheneuc P, Pereon Y.

Muscle Nerve. 2008 Aug;38(2):1055-9.PMID: 18663734 [PubMed - indexed for MEDLINE]Related articles

A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies.

Luigetti M, Conte A, Madia F, Mereu ML, Zollino M, Marangi G, Pomponi MG, Liberatore G, Tonali PA, Sabatelli M.

Muscle Nerve. 2008 Aug;38(2):1060-4.PMID: 18642376 [PubMed - indexed for MEDLINE]Related articles

Hereditary neuropathy with liability to pressure palsies in a Turkish patient (HNPP): a rare cause of entrapment neuropathies in young adults.

Celik Y, Kilinçer C, Hamamcioğlu MK, Balci K, Birgili B, Cobanoğlu S, Utku U.

Turk Neurosurg. 2008 Jan;18(1):82-4.PMID: 18382985 [PubMed - indexed for MEDLINE]Related articlesFree article

A case of rare recessive oculopharyngeal muscular dystrophy (OPMD) coexisting with hereditary neuropathy with liability to pressure palsies (HNPP).

Marsh EA, Robinson DO.

Clin Neurol Neurosurg. 2008 May;110(5):525-8. Epub 2008 Mar 21.PMID: 18358598 [PubMed - indexed for MEDLINE]Related articles

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

Chen SR, Lin KP, Kuo HC, Chen CM, Hsieh ST, Lee MJ, Yang CC, Liu CS, Huang CC, Lyu RK, Ro LS.

Clin Neurol Neurosurg. 2008 May;110(5):466-71. Epub 2008 Mar 18.PMID: 18353535 [PubMed - indexed for MEDLINE]Related articles

A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.

Muglia M, Patitucci A, Rizzi R, Ungaro C, Conforti FL, Gabriele AL, Magariello A, Mazzei R, Motti L, Sabadini R, Sprovieri T, Marcello N, Quattrone A.

J Neurol Sci. 2007 Dec 15;263(1-2):194-7. Epub 2007 Aug 20.PMID: 17707409 [PubMed - indexed for MEDLINE]Related articles

Tomaculous neuropathy in an airline pilot.

Salazar GJ.

Aviat Space Environ Med. 2007 Jul;78(7):720-3.PMID: 17679573 [PubMed - indexed for MEDLINE]Related articles

Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis.

Van Vught PW, Van Wijk J, Bradley TE, Plasmans D, Jakobs ME, Veldink JH, de Jong JM, Van den Berg LH, Baas F.

Neuromuscul Disord. 2007 Dec;17(11-12):964-7. Epub 2007 Jul 24.PMID: 17651970 [PubMed - indexed for MEDLINE]Related articles

Early-onset hereditary neuropathy with liability to pressure palsy.

Antonini G, Luchetti A, Mastrangelo M, Ciambra GL, Di Netta S, Taioli F, Fabrizi GM, Iannetti P.

Neuropediatrics. 2007 Feb;38(1):50-4. Review.PMID: 17607607 [PubMed - indexed for MEDLINE]Related articles

CNS involvement in hereditary neuropathy with pressure palsies (HNPP).

Iwasaki Y, Iguchi H, Ikeda K, Kano O.

Neurology. 2007 Jun 5;68(23):2046. No abstract available. PMID: 17548562 [PubMed - indexed for MEDLINE]Related articles

Rapid diagnosis of CMT1A duplications and HNPP deletions by multiplex microsatellite PCR.

Choi BO, Kim J, Lee KL, Yu JS, Hwang JH, Chung KW.

Mol Cells. 2007 Feb 28;23(1):39-48.PMID: 17464210 [PubMed - indexed for MEDLINE]Related articles

Bilateral hand amyotrophy with PMP-22 gene deletion.

Gochard A, Guennoc AM, Praline J, Malinge MC, de Toffol B, Corcia P.

Eur J Neurol. 2007 Jan;14(1):115-6.PMID: 17222125 [PubMed - indexed for MEDLINE]Related articles

CNS involvement in hereditary neuropathy with pressure palsies (HNPP).

Tackenberg B, Möller JC, Rindock H, Bien S, Sommer N, Oertel WH, Rosenow F, Schepelmann K, Hamer HM, Bandmann O.

Neurology. 2006 Dec 26;67(12):2250-2.PMID: 17190957 [PubMed - indexed for MEDLINE]Related articles