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.
198 related articles for article (PubMed ID: 30922590)
21. [J.M. Charcot 1825-1893. A life of labor]. Sørensen H Dan Medicinhist Arbog; 1996; ():140-58. PubMed ID: 11625138 [TBL] [Abstract][Full Text] [Related]
22. Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome. Stögbauer F; Young P; Wiebusch H; Timmerman V; Kuhlenbäumer G; Nelis E; Ringelstein EB; Kurlemann G; Assmann G; Van Broeckhoven C; Funke H Neurosci Lett; 1998 Jan; 240(1):1-4. PubMed ID: 9488160 [TBL] [Abstract][Full Text] [Related]
23. The Klumpke family--memories by Doctor Déjerine, born Augusta Klumpke. Bogousslavsky J Eur Neurol; 2005; 53(3):113-20. PubMed ID: 15860915 [TBL] [Abstract][Full Text] [Related]
24. Novel mutations of the peripheral myelin protein 22 gene in two pedigrees with Dejerine-Sottas disease. Ikegami T; Ikeda H; Aoyama M; Matsuki T; Imota T; Fukuuchi Y; Amano T; Toyoshima I; Ishihara Y; Endoh H; Hayasaka K Hum Genet; 1998 Mar; 102(3):294-8. PubMed ID: 9544841 [TBL] [Abstract][Full Text] [Related]
25. Figures and institutions of the neurological sciences in Paris from 1800 to 1950. Part III: neurology. Broussolle E; Poirier J; Clarac F; Barbara JG Rev Neurol (Paris); 2012 Apr; 168(4):301-20. PubMed ID: 22387204 [TBL] [Abstract][Full Text] [Related]
27. Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutation. Valentijn LJ; Ouvrier RA; van den Bosch NH; Bolhuis PA; Baas F; Nicholson GA Hum Mutat; 1995; 5(1):76-80. PubMed ID: 7728152 [TBL] [Abstract][Full Text] [Related]
28. Parkinson's disease - the story of an eponym. Goedert M; Compston A Nat Rev Neurol; 2018 Jan; 14(1):57-62. PubMed ID: 29217826 [TBL] [Abstract][Full Text] [Related]
30. Did Jules Dejerine describe AMAN at the end of the 19th century? Mathis S; Magy L; Le Masson G; Vallat JM Neurology; 2017 Oct; 89(16):1749-1753. PubMed ID: 29038133 [TBL] [Abstract][Full Text] [Related]
31. Neuropathology in Pitié-Salpêtrière hospital: Past, present and prospect. Seilhean D Neuropathology; 2020 Feb; 40(1):3-13. PubMed ID: 31802544 [TBL] [Abstract][Full Text] [Related]
32. Observations on hypertrophic neuropathy of Dejerine and Sottas. ANDERMANN F; LLOYD-SMITH DL; MAVOR H; MATHIESON G Neurology; 1962 Oct; 12():712-24. PubMed ID: 13861139 [No Abstract] [Full Text] [Related]
33. Jean-Charles Chatelin (1884-1948), counted among the "Righteous", but forgotten as a neurologist who studied under Pierre Marie. Walusinski O Rev Neurol (Paris); 2020; 176(1-2):43-52. PubMed ID: 31279440 [TBL] [Abstract][Full Text] [Related]
34. Pioneers of movement disorders: Georges Gilles de la Tourette. Krämer H; Daniels C J Neural Transm (Vienna); 2004 Jun; 111(6):691-701. PubMed ID: 15168216 [TBL] [Abstract][Full Text] [Related]
35. Juvenile-onset of Dejerine-Sottas disease in a Taiwanese woman. Liao YS; Chen ST; Tang LM; Ro LS J Formos Med Assoc; 1996 Apr; 95(4):329-32. PubMed ID: 8935304 [TBL] [Abstract][Full Text] [Related]
36. Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene. Jen J; Baloh RH; Ishiyama A; Baloh RW J Neurol Sci; 2005 Oct; 237(1-2):21-4. PubMed ID: 15992829 [TBL] [Abstract][Full Text] [Related]
37. Phrenic nerve involvement in Déjérine-Sottas disease: a clinicopathological case study. Felice KJ; Fratkin JD; Feldman EL; Sima AA Pediatr Pathol; 1994; 14(6):905-11. PubMed ID: 7855009 [TBL] [Abstract][Full Text] [Related]
38. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III. Tachi N; Kozuka N; Ohya K; Chiba S; Naganuma M Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868 [TBL] [Abstract][Full Text] [Related]
40. P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome. Martini R Ann N Y Acad Sci; 1999 Sep; 883():273-80. PubMed ID: 10586252 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]