These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 28357412)

  • 21. Congenital myopathies/dystrophies.
    Riggs JE; Bodensteiner JB; Schochet SS
    Neurol Clin; 2003 Nov; 21(4):779-94; v-vi. PubMed ID: 14743649
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital myopathies.
    Bruno C; Minetti C
    Curr Neurol Neurosci Rep; 2004 Jan; 4(1):68-73. PubMed ID: 14683632
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain.
    Gonzalez-Quereda L; Rodriguez MJ; Diaz-Manera J; Alonso-Perez J; Gallardo E; Nascimento A; Ortez C; Natera-de Benito D; Olive M; Gonzalez-Mera L; Munain AL; Zulaica M; Poza JJ; Jerico I; Torne L; Riera P; Milisenda J; Sanchez A; Garrabou G; Llano I; Madruga-Garrido M; Gallano P
    Genes (Basel); 2020 May; 11(5):. PubMed ID: 32403337
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction.
    Jungbluth H; Treves S; Zorzato F; Sarkozy A; Ochala J; Sewry C; Phadke R; Gautel M; Muntoni F
    Nat Rev Neurol; 2018 Mar; 14(3):151-167. PubMed ID: 29391587
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital myopathies: The current status.
    Goebel HH; Dittmayer C; Stenzel W
    Indian J Pathol Microbiol; 2022 May; 65(Supplement):S271-S276. PubMed ID: 35562159
    [TBL] [Abstract][Full Text] [Related]  

  • 26.
    Avasthi KK; Agarwal S; Panigrahi I
    J Pediatr Neurosci; 2019; 14(4):222-224. PubMed ID: 31908664
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Protein surplus myopathies and other rare congenital myopathies.
    Goebel HH; Borchert A
    Semin Pediatr Neurol; 2002 Jun; 9(2):160-70. PubMed ID: 12139000
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital Myopathies: A Clinicopathological Study of 10 Cases in a Tertiary Care Hospital of North India.
    Maheshwari S; Pant I; Bala K; Paradasani V
    J Pediatr Neurosci; 2021; 16(3):184-195. PubMed ID: 36160617
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neuromuscular transmission defects in myopathies: Rare but worth searching for.
    Elahi B; Laughlin RS; Litchy WJ; Milone M; Liewluck T
    Muscle Nerve; 2019 Apr; 59(4):475-478. PubMed ID: 30536954
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital myopathies in the new millennium.
    Goebel HH
    J Child Neurol; 2005 Feb; 20(2):94-101. PubMed ID: 15794172
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myopathology in congenital myopathies.
    Sewry CA; Wallgren-Pettersson C
    Neuropathol Appl Neurobiol; 2017 Feb; 43(1):5-23. PubMed ID: 27976420
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Electrophysiological study of neuromuscular junction in congenital myasthenic syndromes, congenital myopathies, and chronic progressive external ophthalmoplegia.
    Caldas VM; Heise CO; Kouyoumdjian JA; Zambon AA; Silva AMS; Estephan EP; Zanoteli E
    Neuromuscul Disord; 2020 Nov; 30(11):897-903. PubMed ID: 33121830
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Core myopathies - a short review.
    Topaloglu H
    Acta Myol; 2020 Dec; 39(4):266-273. PubMed ID: 33458581
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trouble at the junction: When myopathy and myasthenia overlap.
    Nicolau S; Kao JC; Liewluck T
    Muscle Nerve; 2019 Dec; 60(6):648-657. PubMed ID: 31449669
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of congenital myopathies at a Korean neuromuscular center.
    Park YE; Shin JH; Kim HS; Lee CH; Kim DS
    Muscle Nerve; 2018 Aug; 58(2):235-244. PubMed ID: 29669168
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Nemaline rod myopathy: a rare form of myopathy.
    Sharma MC; Gulati S; Atri S; Seth R; Kalra V; Das TK; Sarkar C
    Neurol India; 2007; 55(1):70-4. PubMed ID: 17272906
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.
    Nicole S; Chaouch A; Torbergsen T; Bauché S; de Bruyckere E; Fontenille MJ; Horn MA; van Ghelue M; Løseth S; Issop Y; Cox D; Müller JS; Evangelista T; Stålberg E; Ioos C; Barois A; Brochier G; Sternberg D; Fournier E; Hantaï D; Abicht A; Dusl M; Laval SH; Griffin H; Eymard B; Lochmüller H
    Brain; 2014 Sep; 137(Pt 9):2429-43. PubMed ID: 24951643
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital myopathies.
    Bornemann A; Goebel HH
    Brain Pathol; 2001 Apr; 11(2):206-17. PubMed ID: 11303796
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myopathies.
    Srinivasan J; Amato AA
    Phys Med Rehabil Clin N Am; 2003 May; 14(2):403-34, x. PubMed ID: 12795523
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Muscular diseases in relation to drug consumption].
    Uldry PA; Regli F
    Schweiz Rundsch Med Prax; 1989 Jun; 78(23):671-3. PubMed ID: 2568673
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.