SCOPUS 정보 검색 플랫폼

Acta Neurologica Scandinavica

Volumn 94, Issue 1, 1996, Pages 60-62

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions

(7) Malandrini, A a Scarpini, C a Villanova, M a Sicurelli, F a Parrotta, E a DeFalco, D a Guazzi, G C a

a UNIVERSITY OF SIENA (Italy)

Author keywords

Amyotrophy; Autosomal; Recessive; Spastic paraparesis; White matter lesions

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN INJURY; CASE REPORT; FEMALE; HUMAN; MALE; MUSCLE ATROPHY; NUCLEAR MAGNETIC RESONANCE; SPASTIC PARAPLEGIA;

EID: 0029814242 PISSN: 00016314 EISSN: None Source Type: Journal
DOI: 10.1111/j.1600-0404.1996.tb00040.x Document Type: Article

Times cited : (4)

References (9)

1
- 0345478272
- An unusual form of family paralysis
- ORMEROD JA. An unusual form of family paralysis. Lancet 1904: i: 17-18.
- (1904) Lancet , vol.1 , pp. 17-18
- Ormerod, J.A.¹

2
- 9444285605
- Family spastic paralysis associated with amyotrophy
- HOLMES G. Family spastic paralysis associated with amyotrophy. Rev Neurol Psychiat 1905: 3: 256-263.
- (1905) Rev Neurol Psychiat , vol.3 , pp. 256-263
- Holmes, G.¹

3
- 0344184475
- Amyotrophic familial spastic paraplegia
- Minneap.
- REFSUM S, SKJLLICORN SA. Amyotrophic familial spastic paraplegia. Neurology (Minneap.)1954: 4: 40-47.
- (1954) Neurology , vol.4 , pp. 40-47
- Refsum, S.¹ Skjllicorn, S.A.²

4
- 0027314483
- Autosomal recessive paraparesis with amyotrophy of the hands and feet
- BRUYN RPM, SCHELTENS Ph, LYCKLAMA À NUEHOLT J, DE JONG JMBV. Autosomal recessive paraparesis with amyotrophy of the hands and feet. Acta Neurol Scand 1993: 87: 443-445.
- (1993) Acta Neurol Scand , vol.87 , pp. 443-445
- Bruyn, R.P.M.¹ Scheltens, Ph.² Lycklama, À.³ Nueholt, J.⁴ De Jong, J.M.B.V.⁵

5
- 0025237394
- Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis)
- BEN HAMIDA M, HENTATI F, BEN HAMIDA C. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Brain 1990: 113: 347-363.
- (1990) Brain , vol.113 , pp. 347-363
- Ben Hamida, M.¹ Hentati, F.² Ben Hamida, C.³

6
- 0028334717
- Linkage of recessive familial lateral sclerosis to chromosome 2q33-q35
- HENTATI A, BFJAOUI K, PERICAK-VANCE MA et al. Linkage of recessive familial lateral sclerosis to chromosome 2q33-q35. Nature Genet 1994: 7: 425-428.
- (1994) Nature Genet , vol.7 , pp. 425-428
- Hentati, A.¹ Bfjaoui, K.² Pericak-Vance, M.A.³

7
- 0025327675
- Complicated hereditary spastic paraparesis with cerebral white matter lesions
- GUTMANN DH, FISCHBECK KH, KAMHOLZ J. Complicated hereditary spastic paraparesis with cerebral white matter lesions. Am J Med Genet 1990: 36: 251-257.
- (1990) Am J Med Genet , vol.36 , pp. 251-257
- Gutmann, D.H.¹ Fischbeck, K.H.² Kamholz, J.³

8
- 9444256110
- Descrizione di 4 casi sporadici di paraparesi spastica di tipo abiotrofico associata ad alterazioni bilaterali della sostanza bianca periventricolare e dei centri semiovali
- MALANDRINI A, CIACCI G, PALMERI S, GUAZZI GC. Descrizione di 4 casi sporadici di paraparesi spastica di tipo abiotrofico associata ad alterazioni bilaterali della sostanza bianca periventricolare e dei centri semiovali. Neuroradiologia 1992: 451-456.
- (1992) Neuroradiologia , pp. 451-456
- Malandrini, A.¹ Ciacci, G.² Palmeri, S.³ Guazzi, G.C.⁴

9
- 0004643472
- Familial spastic paraplegia with amyotrophy, oligophrenia and central retinal degeneration
- KJELLIN KG. Familial spastic paraplegia with amyotrophy, oligophrenia and central retinal degeneration. Arch Neurol 1959: 1: 133-140.
- (1959) Arch Neurol , vol.1 , pp. 133-140
- Kjellin, K.G.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.