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Journal Abstract Search

126 related items for PubMed ID: 3420560

  • 1. Diaphragm weakness in Charcot-Marie-Tooth disease.
    Laroche CM, Carroll N, Moxham J, Stanley NN, Evans RJ, Green M.
    Thorax; 1988 Jun; 43(6):478-9. PubMed ID: 3420560
    [Abstract] [Full Text] [Related]

  • 2. Respiratory muscle weakness in Charcot-Marie-Tooth disease. A field study.
    Nathanson BN, Yu DG, Chan CK.
    Arch Intern Med; 1989 Jun; 149(6):1389-91. PubMed ID: 2730255
    [Abstract] [Full Text] [Related]

  • 3. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).
    Chan CK, Mohsenin V, Loke J, Virgulto J, Sipski ML, Ferranti R.
    Chest; 1987 Apr; 91(4):567-70. PubMed ID: 3829750
    [Abstract] [Full Text] [Related]

  • 4. Phrenic nerve involvement and respiratory muscle weakness in patients with Charcot-Marie-Tooth disease 1A.
    Spiesshoefer J, Henke C, Kabitz HJ, Akova-Oeztuerk E, Draeger B, Herkenrath S, Randerath W, Young P, Brix T, Boentert M.
    J Peripher Nerv Syst; 2019 Sep; 24(3):283-293. PubMed ID: 31393643
    [Abstract] [Full Text] [Related]

  • 5. Charcot-Marie-Tooth disease with diaphragmatic weakness.
    Osanai S, Akiba Y, Nakano H, Matsumoto H, Yahara O, Onodera S.
    Intern Med; 1992 Nov; 31(11):1267-70. PubMed ID: 1295621
    [Abstract] [Full Text] [Related]

  • 6. Respiratory muscle dysfunction in hereditary neuropathy.
    Hogan GR.
    Arch Intern Med; 1988 Aug; 148(8):1707-8. PubMed ID: 3401090
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type I.
    Eichacker PQ, Spiro A, Sherman M, Lazar E, Reichel J, Dodick F.
    Arch Intern Med; 1988 Aug; 148(8):1739-40. PubMed ID: 3401096
    [Abstract] [Full Text] [Related]

  • 9. Pathophysiology of Charcot-Marie-Tooth disease.
    Mann RA, Missirian J.
    Clin Orthop Relat Res; 1988 Sep; (234):221-8. PubMed ID: 3409580
    [Abstract] [Full Text] [Related]

  • 10. Electrophysiological study (EEG, VEPs, BAEPs) in patients with Charcot Marie Tooth (type HMSN I) disease.
    Triantafyllou N, Rombos A, Athanasopoulou H, Siafakas A, Loulakaki SM.
    Electromyogr Clin Neurophysiol; 1989 Sep; 29(5):259-63. PubMed ID: 2766989
    [Abstract] [Full Text] [Related]

  • 11. Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case.
    Kulshrestha R, Forrester N, Antoniadi T, Willis T, Sethuraman SK, Samuels M.
    Neuromuscul Disord; 2018 Dec; 28(12):1016-1021. PubMed ID: 30409445
    [Abstract] [Full Text] [Related]

  • 12. [Carbamazepine-sensitive neuromyotonia and Charcot-Marie-Tooth disease of the neuronal type].
    Serratrice G, Pouget J, Pellissier JF, Cros D.
    Rev Neurol (Paris); 1989 Dec; 145(12):867-8. PubMed ID: 2694289
    [Abstract] [Full Text] [Related]

  • 13. Phrenic nerve involvement in Charcot-Marie-Tooth disease.
    Abboud L, El SF, Takubo T, Byrd RP, Roy TM.
    Tenn Med; 2005 Oct; 98(10):495-7. PubMed ID: 16294569
    [Abstract] [Full Text] [Related]

  • 14. Disorders of pulmonary function, sleep, and the upper airway in Charcot-Marie-Tooth disease.
    Aboussouan LS, Lewis RA, Shy ME.
    Lung; 2007 Oct; 185(1):1-7. PubMed ID: 17294338
    [Abstract] [Full Text] [Related]

  • 15. Neurofibromatosis, Charcot-Marie-Tooth disease, or both?
    Roos KL, Pascuzzi RM, Dunn DW.
    Neurofibromatosis; 1989 Oct; 2(4):238-43. PubMed ID: 2517818
    [Abstract] [Full Text] [Related]

  • 16. Motor unit recruitment order in neuropathic disease.
    Herdmann J, Reiners K, Freund HJ.
    Electromyogr Clin Neurophysiol; 1988 Jan; 28(1):53-60. PubMed ID: 2844503
    [No Abstract] [Full Text] [Related]

  • 17. [Progressive neuropathic muscular atrophy with pattern reversal visual evoked potentials].
    Cao PZ.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1987 Oct; 20(5):286-9. PubMed ID: 3450486
    [No Abstract] [Full Text] [Related]

  • 18. Charcot-Marie-Tooth disease.
    Martel J, Mierau D, Donat J.
    J Manipulative Physiol Ther; 1995 Oct; 18(3):168-71. PubMed ID: 7790797
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F, Espinós C.
    Brain; 2016 Jan; 139(Pt 1):62-72. PubMed ID: 26497905
    [Abstract] [Full Text] [Related]

  • 20. Phrenic involvement in Charcot-Marie-Tooth disease. A pathologic documentation.
    Gilchrist D, Chan CK, Deck JH.
    Chest; 1989 Nov; 96(5):1197-9. PubMed ID: 2553346
    [Abstract] [Full Text] [Related]

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