119 related articles for article (PubMed ID: 8433609)
1. [The men behind the syndrome: Werdnig and Hoffmann. They classified spinal muscular atrophies].
Fogström B; Bui TH
Lakartidningen; 1993 Jan; 90(4):275-6. PubMed ID: 8433609
[No Abstract] [Full Text] [Related]
2. An early description of monomelic amyotrophy: An excerpt from the diaries of Dr. Charles I Smith (1830-1880) in Bangalore, Southern India.
Jain S
Neurol India; 2017; 65(1):11-13. PubMed ID: 28084229
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.
Melki J; Abdelhak S; Burlet P; Raclin V; Kaplan J; Spiegel R; Gilgenkrantz S; Philip N; Chauvet ML; Dumez Y
J Med Genet; 1992 Mar; 29(3):171-4. PubMed ID: 1348092
[TBL] [Abstract][Full Text] [Related]
5. [Two cases of Werdnig-Hofmann disease].
Palmer-Morales Y; Pacheco-Flores G; Ames-Guevara Y; Gaxiola-Apodaca M; Gaspar-Franco D; Landavazo-Acuña G; Hernández-Rocha F
Rev Med Inst Mex Seguro Soc; 2010; 48(3):317-9. PubMed ID: 21192906
[TBL] [Abstract][Full Text] [Related]
6. An unusual neurologic problem: Werdnig-Hoffmann disease.
Barden C; Lee R; Parchment Y; Dempsey RM
Crit Care Nurse; 1990; 10(10):60-7. PubMed ID: 2249464
[TBL] [Abstract][Full Text] [Related]
7. Two early infantile hereditary cases of progressive muscular atrophy simulating dystrophy, but on a neural basis. 1891.
Werdnig G
Arch Neurol; 1971 Sep; 25(3):276-8. PubMed ID: 4952838
[No Abstract] [Full Text] [Related]
8. [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]
9. [Werdnig-Hoffmann amyotrophy in a 7-month-old child].
Kutafin IuF; Osipov SM
Pediatriia; 1990; (4):91-3. PubMed ID: 2371136
[No Abstract] [Full Text] [Related]
10. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
Feng J; Toshiyuki Y
Chin Med J (Engl); 2003 May; 116(5):673-5. PubMed ID: 12875676
[TBL] [Abstract][Full Text] [Related]
11. MR findings of Werdnig-Hoffmann disease in two infants.
Hsu CF; Chen CY; Yuh YS; Chen YH; Hsu YT; Zimmerman RA
AJNR Am J Neuroradiol; 1998 Mar; 19(3):550-2. PubMed ID: 9541317
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. [Werdnig-Hoffmann's congenital spinal atrophy in nursing infants].
Kutafin IuF; Osipov SM; Osipov ES
Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):15-8. PubMed ID: 1646528
[TBL] [Abstract][Full Text] [Related]
14. [Two cases of a proximal spinal muscular atrophy (Werdnig-Hoffmann's disease) in one family].
Nurbekova UA
Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(10):106-7. PubMed ID: 25591528
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes.
Stipoljev F; Sertić J; Latin V; Rukavina-Stavljenić A; Kurjak A
Croat Med J; 1999 Sep; 40(3):433-7. PubMed ID: 10411975
[TBL] [Abstract][Full Text] [Related]
17. Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen).
Thieme A; Mitulla B; Schulze F; Spiegler AW
Hum Genet; 1993 Apr; 91(3):295-7. PubMed ID: 8478016
[TBL] [Abstract][Full Text] [Related]
18. Johann Hoffmann (1857-1919).
Mahmoudi Nezhad GS; Dalfardi B
J Neurol; 2014 Sep; 261(9):1848-9. PubMed ID: 24158276
[No Abstract] [Full Text] [Related]
19. 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]
20. Amyotonia congenita syndrome, with the report of a case of Werdnig-Hoffmann disease.
SINGH R; PRASAD R; MATHUR GP; KALRA K
Indian J Pediatr; 1963 Apr; 30():118-21. PubMed ID: 13977661
[No Abstract] [Full Text] [Related]
[Next] [New Search]