120 related articles for article (PubMed ID: 7807154)
1. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
Camu W; Billiard M
J Neurol Sci; 1994 Jul; 124 Suppl():88-9. PubMed ID: 7807154
[No Abstract] [Full Text] [Related]
2. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
Appelbaum JS; Roos RP
Muscle Nerve; 1993 Dec; 16(12):1416. PubMed ID: 8232401
[No Abstract] [Full Text] [Related]
3. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
Camu W; Billiard M
Muscle Nerve; 1993 May; 16(5):569-70. PubMed ID: 8515770
[No Abstract] [Full Text] [Related]
4. Peripheral nerve involvement in Werdnig-Hoffmann disease.
Chien YY; Nonaka I
Brain Dev; 1989; 11(4):221-9. PubMed ID: 2774090
[TBL] [Abstract][Full Text] [Related]
5. Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family.
Shaw PJ; Ince PG; Goodship J; Burn J; Slade J; Bates D; Medwin DG
Neurology; 1992 Aug; 42(8):1477-80. PubMed ID: 1641139
[TBL] [Abstract][Full Text] [Related]
6. Controversy over Werdnig-Hoffmann disease and multiple system atrophy.
Chou SM
Curr Opin Neurol; 1993 Dec; 6(6):861-4. PubMed ID: 8293160
[No Abstract] [Full Text] [Related]
7. Heterotopic neurons in amyotrophic lateral sclerosis.
Martin JE; Mather K; Swash M
Neurology; 1993 Jul; 43(7):1420-2. PubMed ID: 8327148
[TBL] [Abstract][Full Text] [Related]
8. [Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].
Cneude F; Sukno S; Boidein F; Dehouck MB; Bourlet A; Vittu G
Rev Neurol (Paris); 1999 Sep; 155(8):589-91. PubMed ID: 10486849
[TBL] [Abstract][Full Text] [Related]
9. Ubiquitin and phosphorylated neurofilament epitopes in ballooned neurons of the extraocular muscle nuclei in a case of Werdnig-Hoffmann disease.
Kato S; Hirano A
Acta Neuropathol; 1990; 80(3):334-7. PubMed ID: 1698008
[TBL] [Abstract][Full Text] [Related]
10. Ubiquitin-positive inclusion in anterior horn cells in subgroups of motor neuron diseases: a comparative study of adult-onset amyotrophic lateral sclerosis, juvenile amyotrophic lateral sclerosis and Werdnig-Hoffmann disease.
Matsumoto S; Goto S; Kusaka H; Imai T; Murakami N; Hashizume Y; Okazaki H; Hirano A
J Neurol Sci; 1993 Apr; 115(2):208-13. PubMed ID: 8387100
[TBL] [Abstract][Full Text] [Related]
11. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R
Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861
[No Abstract] [Full Text] [Related]
12. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
Boylan KB; Cornblath DR
Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
[TBL] [Abstract][Full Text] [Related]
13. Brain atrophy in Werdnig-Hoffmann disease.
Yohannan M; Patel P; Kolawole T; Malabarey T; Mahdi A
Acta Neurol Scand; 1991 Nov; 84(5):426-8. PubMed ID: 1776391
[TBL] [Abstract][Full Text] [Related]
14. Werdnig-Hoffmann disease with congenital hypothyroidism.
Gunes T; Akcakus M; Cetin N; Kurtoğlu S; Kumandaş S
Ann Trop Paediatr; 2003 Dec; 23(4):301-4. PubMed ID: 14738578
[TBL] [Abstract][Full Text] [Related]
15. Synaptic alterations of anterior horn cells in Werdnig-Hoffmann disease.
Yamanouchi Y; Yamanouchi H; Becker LE
Pediatr Neurol; 1996 Jul; 15(1):32-5. PubMed ID: 8858698
[TBL] [Abstract][Full Text] [Related]
16. Histochemistry and morphometry of Werdnig-Hoffmann disease.
Artacho Pérula E; Roldán Villalobos R; Vaamonde Lemos R
Histol Histopathol; 1989 Jul; 4(3):265-70. PubMed ID: 2485193
[TBL] [Abstract][Full Text] [Related]
17. Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann disease.
Vajsar J; Balslev T; Ray PN; Siegel-Bartelt J; Jay V
Neurology; 1998 Sep; 51(3):873-5. PubMed ID: 9748045
[TBL] [Abstract][Full Text] [Related]
18. Transient cytoplasmic bodies in muscle of three infants with Werdnig-Hoffmann disease.
Buchino JJ; Bove KE; Iannaccone ST
Pediatr Pathol; 1990; 10(4):563-73. PubMed ID: 2164661
[TBL] [Abstract][Full Text] [Related]
19. [Spinal muscular atrophy in young infants].
Smit LM; Hageman EG
Tijdschr Kindergeneeskd; 1989 Jun; 57(3):102-6. PubMed ID: 2799798
[TBL] [Abstract][Full Text] [Related]
20. Chromatolytic neurons in Werdnig-Hoffmann disease contain phosphorylated neurofilaments.
Lippa CF; Smith TW
Acta Neuropathol; 1988; 77(1):91-4. PubMed ID: 3149123
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
