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3. [Chronic X-linked recessive bulbospinal amyotrophy (Kennedy-Stefanis type). Apropos of a case]. Serratrice G; Guastalla P Sem Hop; 1984 Mar; 60(14):1003-5. PubMed ID: 6326279 [TBL] [Abstract][Full Text] [Related]
4. [Family with progressive myelopathic muscular atrophy with proximal distribution and onset in adulthood]. Mapelli G Riv Patol Nerv Ment; 1983; 104(4):159-70. PubMed ID: 6681331 [TBL] [Abstract][Full Text] [Related]
5. Wohlfart Kugelberg Welander syndrome. Ross RT; Simpson CA; Styles S Can J Neurol Sci; 1974 May; 1(2):130-8. PubMed ID: 4434270 [No Abstract] [Full Text] [Related]
8. [Histological-histochemical studies on muscular changes in pseudomyopathic spinal muscular atrophy (Wohlfart-Kugelberg-Welander)]. Heene R Z Neurol; 1970; 198(3):291-304. PubMed ID: 4102127 [No Abstract] [Full Text] [Related]
9. [Hereditary proximal neurogenic muscular atrophy (Wohlfart-Kugelberg-Welander disease). Electromyographic, anatomo-pathologic and clinical study in 3 brothers]. De Freitas MR; Nascimento OJ Arq Neuropsiquiatr; 1976 Mar; 34(1):81-8. PubMed ID: 1259636 [TBL] [Abstract][Full Text] [Related]
10. Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree. Tsukagoshi H; Shoji H; Furukawa T Neurology; 1970 Dec; 20(12):1188-93. PubMed ID: 5529907 [No Abstract] [Full Text] [Related]
11. [Cumulative familial incidence of Kugelberg-Welander disease]. Nemes A; Károly E; Csenkér E; Pintér S Orv Hetil; 1986 Nov; 127(45):2735-9. PubMed ID: 3796971 [No Abstract] [Full Text] [Related]
12. X-linked recessive bulbospinal neuronopathy: a report of ten cases. Harding AE; Thomas PK; Baraitser M; Bradbury PG; Morgan-Hughes JA; Ponsford JR J Neurol Neurosurg Psychiatry; 1982 Nov; 45(11):1012-9. PubMed ID: 6890989 [TBL] [Abstract][Full Text] [Related]
13. Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases. Ghetti B; Amati A; Turra MV; Pacini A; Del Vecchio M; Guazzi GC Acta Genet Med Gemellol (Roma); 1971 Jan; 20(1):43-58. PubMed ID: 5568110 [No Abstract] [Full Text] [Related]
14. [A case of Wohlfart-Kugelberg-Welander disease or hereditary familial spinal juvenile muscular atrophy]. Manara F; Gasco P; Milani L Minerva Med; 1977 Feb; 68(6):417-24. PubMed ID: 840437 [No Abstract] [Full Text] [Related]
15. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait. Kennedy WR; Alter M; Sung JH Neurology; 1968 Jul; 18(7):671-80. PubMed ID: 4233749 [No Abstract] [Full Text] [Related]
16. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease). Fried K; Emery AE Clin Genet; 1971; 2(4):203-9. PubMed ID: 5146579 [No Abstract] [Full Text] [Related]
17. [Case of progressive proximal spinal and bulbar muscular atrophy of late onset (Kennedy-Alter-Sung) with gynecomastia, tremors (of the fingers and head), muscle cramps and pains of the lower back and extremities]. Araki S; Ushio K Rinsho Shinkeigaku; 1972 Jan; 12(1):9-14. PubMed ID: 4264884 [No Abstract] [Full Text] [Related]
18. [Sporadic proximal spinal amyotrophy (Kugelberg-Welander) with a late onset. Its place in the framework degenerations]. de Barsy T; Hariga J; Claes C Encephale; 1966; 55(6):541-57. PubMed ID: 5982328 [No Abstract] [Full Text] [Related]
19. [The Wohlfart-Kugelberg-Welander disease. A clinical case with nonobstructive myocardiopathy]. Lagarde P; Bakouche P; Lamotte-Barrillon S Sem Hop; 1976 Apr; 52(16):1017-21. PubMed ID: 188171 [No Abstract] [Full Text] [Related]