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.
24. [Diaphragmatic paralysis in the Parsonage-Turner syndrome]. Pou Serradell A Rev Clin Esp; 1986 May; 178(9):463-4. PubMed ID: 3738035 [No Abstract] [Full Text] [Related]
25. [The neuralgic shoulder myatrophy. The differential diagnosis of shoulder-arm syndromes]. Scherer PW; Baum KA Dtsch Med Wochenschr; 1995 Mar; 120(11):371-4. PubMed ID: 7889819 [No Abstract] [Full Text] [Related]
26. [Complete and fruste forms of the Parsonage and Turner syndrome]. Recordier AM; Serratrice G; Roux H; Acquaviva P Mars Med; 1965; 102(7):597-600. PubMed ID: 5855128 [No Abstract] [Full Text] [Related]
27. Severe bilateral atrophy of the spinati muscles in a cadaver. Tubbs RS; Salter EG; Oakes WJ Folia Morphol (Warsz); 2005 Aug; 64(3):224-5. PubMed ID: 16228959 [TBL] [Abstract][Full Text] [Related]
28. [Contribution to the clinical study of the Parsonage and Turner syndrome. 15 personal observations (author's transl)]. PouSerradell A Acta Neurol Belg; 1975; 75(1):15-23. PubMed ID: 1202893 [TBL] [Abstract][Full Text] [Related]
29. [A case of flexion myelopathy presenting with reversible muscular weakness and atrophy of the unilateral proximal upper limb]. Ando T; Fukatsu H; Kameyama T; Takahashi A; Yamada H Rinsho Shinkeigaku; 1993 May; 33(5):575-8. PubMed ID: 8365071 [TBL] [Abstract][Full Text] [Related]
32. [Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies]. Herrmann V Padiatr Grenzgeb; 1983; 22(1):27-45. PubMed ID: 6866527 [No Abstract] [Full Text] [Related]
33. [Case of Parsonage-Turner syndrome]. Sopek M; Slizewski M; Jodczyk KJ Neurol Neurochir Pol; 1972; 6(1):127-30. PubMed ID: 5018103 [No Abstract] [Full Text] [Related]
34. Comment on "delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literature" by Azzolini S et al. Brain & Development 2014;36:716-720. Yamamoto T; Takanashi J; Kurosawa K; Deguchi K; Osaka H; Inoue K Brain Dev; 2015 Nov; 37(10):988-9. PubMed ID: 25863745 [No Abstract] [Full Text] [Related]
36. The Value of Comprehensive Thyroid Function Testing and Family History for Early Diagnosis of MCT8 Deficiency. Bedoyan JK; Tim-Aroon T; Deeb KK; Ganganna ST; Bass NE Clin Pediatr (Phila); 2016 Mar; 55(3):286-9. PubMed ID: 25926664 [No Abstract] [Full Text] [Related]
37. Parsonage-Turner syndrome after total-hip arthroplasty. Simon JP; Fabry G J Arthroplasty; 2001 Jun; 16(4):518-20. PubMed ID: 11402420 [TBL] [Abstract][Full Text] [Related]
38. Bilateral Parsonage-Turner syndrome with unilateral brachialis muscle wasting: a case report. Van Tongel A; Schreurs M; Bruyninckx F; Debeer P J Shoulder Elbow Surg; 2010 Dec; 19(8):e14-6. PubMed ID: 20630777 [No Abstract] [Full Text] [Related]
39. [On the clinical picture of the neuralgic amyotrophy (Syndrom of Parsonage and Turner)]. Wieczorek V; Jung H Nervenarzt; 1965 Jul; 36(7):318-9. PubMed ID: 5841921 [No Abstract] [Full Text] [Related]