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Annals of the New York Academy of Sciences

Volumn 883, Issue , 1999, Pages 445-448

A second family with autosomal dominant burning feet syndrome

(10) Kuhlenbaumer G a,b Young, P b Kiefer, R b Timmerman, V a Wang, J F c Schroeder, J M c Weis, J d Ringelstein, E B b Van Broeckhoven, C a Stoegbauer, F b

a UNIVERSITY OF ANTWERP (Belgium)

b UNIVERSITY OF MÜNSTER (Germany)

c RWTH AACHEN UNIVERSITY (Germany)

d UNIVERSITY OF BERN (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 9; CHROMOSOME MAP; DOMINANT GENE; FEMALE; FOOT DISEASE; GENETIC LINKAGE; GENETICS; GERMANY; HUMAN; MALE; NEUROPATHY; PEDIGREE; SYNDROME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FOOT DISEASES; GENES, DOMINANT; GERMANY; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; LOD SCORE; MALE; PEDIGREE; SYNDROME;

EID: 0033554324 PISSN: 00778923 EISSN: None Source Type: Book Series
DOI: 10.1111/j.1749-6632.1999.tb08606.x Document Type: Article

Times cited : (9)

References (5)

1
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- "Burning feet" as the only manifestation of dominantly inherited sensory neuropathy
- DYCK, R.J., P.A. Low & J.C. STEVENS. 1983. "Burning feet" as the only manifestation of dominantly inherited sensory neuropathy. Mayo Clin. Proc. 58: 426-429.
- (1983) Mayo Clin. Proc. , vol.58 , pp. 426-429
- Dyck, R.J.¹ Low, P.A.² Stevens, J.C.³

2
- 0030140392
- The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3
- NICHOLSON, G.A., J.L. DAWKINS, I.P. BLAIR, M.L. KENNERSON, M.J. GORDON, A.K. CHERRYSON, J. NASH & T. BANANIS. 1996. The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3. Nat. Genet. 13: 101-114.
- (1996) Nat. Genet. , vol.13 , pp. 101-114
- Nicholson, G.A.¹ Dawkins, J.L.² Blair, I.P.³ Kennerson, M.L.⁴ Gordon, M.J.⁵ Cherryson, A.K.⁶ Nash, J.⁷ Bananis, T.⁸

3
- 0029150128
- Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q
- KWON, J.M., J.L. ELLIOTT, W.C. YEE, J. IVANOVICH, N.J. SCAVARDA, P.J. MOOLSINTONG & P.J. GOODFELLOW. 1995. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Am. J. Hum. Genet. 57: 853-858.
- (1995) Am. J. Hum. Genet. , vol.57 , pp. 853-858
- Kwon, J.M.¹ Elliott, J.L.² Yee, W.C.³ Ivanovich, J.⁴ Scavarda, N.J.⁵ Moolsintong, P.J.⁶ Goodfellow, P.J.⁷

4
- 0029984734
- Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy
- SCHRODER, J.M., M. MAYER & J. WEIS. 1996. Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy. Acta Neuropathol. (Berlin). 92: 64-69.
- (1996) Acta Neuropathol. (Berlin) , vol.92 , pp. 64-69
- Schroder, J.M.¹ Mayer, M.² Weis, J.³

5
- 0030928374
- Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family
- DE JONGHE, P., V. TIMMERMAN, D. FITZPATRICK, P. SPOELDERS, J.J. MARTIN & C. VAN BROECKHOVEN. 1997. Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family. J. Neurol. Neurosurg. Psychiatry 62: 570-573.
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