-
1
-
-
0020073371
-
Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1
-
Bird T.D., Ott J., Giblett E.R. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. Am J Hum Genet. 34:1982;388-394.
-
(1982)
Am J Hum Genet
, vol.34
, pp. 388-394
-
-
Bird, T.D.1
Ott, J.2
Giblett, E.R.3
-
2
-
-
0030993366
-
Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: A 20-year study
-
Bird T.D., Kraft G.H., Lipe H.P., Kennev K.L., Sumi S.M. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study. Ann Neurol. 41:1997;463-469.
-
(1997)
Ann Neurol
, vol.41
, pp. 463-469
-
-
Bird, T.D.1
Kraft, G.H.2
Lipe, H.P.3
Kennev, K.L.4
Sumi, S.M.5
-
3
-
-
0001046663
-
Hereditary motor and sensory neuropathies
-
P.J. Dyck, & P.K. Thomas. Philadelphia: WB Saunders
-
Dyck P.J., Chance P., Lebo R., Carney J.A. Hereditary motor and sensory neuropathies. Dyck P.J., Thomas P.K. Peripheral neuropathy. 3rd ed. 1993;1094-1136 WB Saunders, Philadelphia.
-
(1993)
Peripheral Neuropathy 3rd Ed.
, pp. 1094-1136
-
-
Dyck, P.J.1
Chance, P.2
Lebo, R.3
Carney, J.A.4
-
4
-
-
0027221141
-
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin Po gene
-
Hayasaka K., Himoro M., Sato W., Takada G., Uyemura K., Shimizu N., Bird T., Conneally P.M., Chance P.F. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin Po gene. Nat Genet. 5:1993;31-34.
-
(1993)
Nat Genet
, vol.5
, pp. 31-34
-
-
Hayasaka, K.1
Himoro, M.2
Sato, W.3
Takada, G.4
Uyemura, K.5
Shimizu, N.6
Bird, T.7
Conneally, P.M.8
Chance, P.F.9
-
5
-
-
0029873432
-
Correlation between histologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood
-
Ouvrier R. Correlation between histologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood. J Child Neurol. 11:1996;133-146.
-
(1996)
J Child Neurol
, vol.11
, pp. 133-146
-
-
Ouvrier, R.1
-
6
-
-
0028847995
-
Charcot-Marie-Tooth neuropathies: From clinical description to molecular genetics
-
Ionasescu V.V. Charcot-Marie-Tooth neuropathies: from clinical description to molecular genetics. Muscle Nerve. 18:1995;267-275.
-
(1995)
Muscle Nerve
, vol.18
, pp. 267-275
-
-
Ionasescu, V.V.1
-
7
-
-
0025868571
-
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
-
Lupski J.R., de Oca-Luna R.M., Slaugenhaupt S., Pentato L., Guzzetta V., Trask B.J., Saucedo-Cardenas O., Barker D.F., Killian J.M., Garcia C.A., Chakravarti A., Patel P.I. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell. 66:1991;219-232.
-
(1991)
Cell
, vol.66
, pp. 219-232
-
-
Lupski, J.R.1
De Oca-Luna, R.M.2
Slaugenhaupt, S.3
Pentato, L.4
Guzzetta, V.5
Trask, B.J.6
Saucedo-Cardenas, O.7
Barker, D.F.8
Killian, J.M.9
Garcia, C.A.10
Chakravarti, A.11
Patel, P.I.12
-
8
-
-
0032948117
-
Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies
-
Nelis E., Haites N., Van Broeckhoven C. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. Hum Mutat. 13:1999;11-28.
-
(1999)
Hum Mutat
, vol.13
, pp. 11-28
-
-
Nelis, E.1
Haites, N.2
Van Broeckhoven, C.3
-
9
-
-
0030897325
-
De novo mutation (Arg98→Cys) of the myelin Po gene and uncompaction of major dense line of the myelin sheath in a severe variant of Charcot-Marie-Tooth disease type 1B
-
Komiyama A., Ohnishi A., Izawa K., Yamamori S., Ohashi H., Hasegawa O. De novo mutation (Arg98→Cys) of the myelin Po gene and uncompaction of major dense line of the myelin sheath in a severe variant of Charcot-Marie-Tooth disease type 1B. J Neurol Sci. 149:1997;103-109.
-
(1997)
J Neurol Sci
, vol.149
, pp. 103-109
-
-
Komiyama, A.1
Ohnishi, A.2
Izawa, K.3
Yamamori, S.4
Ohashi, H.5
Hasegawa, O.6
-
10
-
-
0041114444
-
Two divergent types of nerve pathology in patients with different Po mutations in Charcot-Marie-Tooth disease
-
Gabreëls-Festen A.A.W.M., Hoogendijk J.E., Meijerink P.H.S., Gabreels F.J.M., Bolhuis P.A., van Beersum S., Kulkens T., Nelis E., Jennekens F.G.I., de Visser M., van Engelen B.G.M., Van Broeckhoven C., Mariman E.C.M. Two divergent types of nerve pathology in patients with different Po mutations in Charcot-Marie-Tooth disease. Neurology. 47:1996;761-765.
-
(1996)
Neurology
, vol.47
, pp. 761-765
-
-
Gabreëls-Festen, A.A.W.M.1
Hoogendijk, J.E.2
Meijerink, P.H.S.3
Gabreels, F.J.M.4
Bolhuis, P.A.5
Van Beersum, S.6
Kulkens, T.7
Nelis, E.8
Jennekens, F.G.I.9
De Visser, M.10
Van Engelen, B.G.M.11
Van Broeckhoven, C.12
Mariman, E.C.M.13
-
11
-
-
0028079552
-
Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome
-
Thomas F.P., Lebo R.V., Rosoklija G., Ding X.-S., Lovelace R.E., Latov N., Hays A.P. Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome. Acta Neuropathol. 87:1994;91-97.
-
(1994)
Acta Neuropathol
, vol.87
, pp. 91-97
-
-
Thomas, F.P.1
Lebo, R.V.2
Rosoklija, G.3
Ding, X.-S.4
Lovelace, R.E.5
Latov, N.6
Hays, A.P.7
-
12
-
-
0019161221
-
Human diabetic endoneurial sorbitol, fructose and myo-inositol related to sural nerve morphometry
-
Dyck P.J., Sherman W.R., Hallcher L.M., Service F.J., O'Brien P.C., Grina L.A., Palumbo P.J., Swanson C.J. Human diabetic endoneurial sorbitol, fructose and myo-inositol related to sural nerve morphometry. Ann Neurol. 8:1980;590-596.
-
(1980)
Ann Neurol
, vol.8
, pp. 590-596
-
-
Dyck, P.J.1
Sherman, W.R.2
Hallcher, L.M.3
Service, F.J.4
O'Brien, P.C.5
Grina, L.A.6
Palumbo, P.J.7
Swanson, C.J.8
-
13
-
-
0026879614
-
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
-
Patel P.I., Roa B.B., Welcher A.A., Schoener-Scott R., Trask B.J., Pentao L., Snipes J., Garcia C.A., Francke U., Shooter E.M., Lupski J.R., Suter U. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nat Genet. 1:1992;159-165.
-
(1992)
Nat Genet
, vol.1
, pp. 159-165
-
-
Patel, P.I.1
Roa, B.B.2
Welcher, A.A.3
Schoener-Scott, R.4
Trask, B.J.5
Pentao, L.6
Snipes, J.7
Garcia, C.A.8
Francke, U.9
Shooter, E.M.10
Lupski, J.R.11
Suter, U.12
-
14
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita M., Iwahana H., Kanazawa H., Hayashi K., Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci USA. 86:1989;2766-2770.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
15
-
-
0025833803
-
Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin
-
Hayasaka K., Nanao K., Tahara M., Sato W., Takada G., Miura M., Uyemura K. Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin. Biochem Biophys Res Commun. 180:1991;515-518.
-
(1991)
Biochem Biophys Res Commun
, vol.180
, pp. 515-518
-
-
Hayasaka, K.1
Nanao, K.2
Tahara, M.3
Sato, W.4
Takada, G.5
Miura, M.6
Uyemura, K.7
-
16
-
-
0029959083
-
Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies
-
Meijerink P.H.S., Hoogendijk J.E., Gabreëls-Festen A.A.W.M., Zorn I., Veldinan H., Baas F., de Visser M., Bolhuis P.A. Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies. Ann Neurol. 40:1996;672-675.
-
(1996)
Ann Neurol
, vol.40
, pp. 672-675
-
-
Meijerink, P.H.S.1
Hoogendijk, J.E.2
Gabreëls-Festen, A.A.W.M.3
Zorn, I.4
Veldinan, H.5
Baas, F.6
De Visser, M.7
Bolhuis, P.A.8
-
17
-
-
16044362374
-
Clinical phenotypes of different MPZ (Po) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
-
Warner L.E., Hilz M.J., Appel S., Killian J.M., Kolody E.H., Karpati G., Carpenter S., Watters G.V., Wheeler C., Witt D., Bodell A., Nelis E., Van Broeckhoven C., Lupski J.R. Clinical phenotypes of different MPZ (Po) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron. 17:1996;451-460.
-
(1996)
Neuron
, vol.17
, pp. 451-460
-
-
Warner, L.E.1
Hilz, M.J.2
Appel, S.3
Killian, J.M.4
Kolody, E.H.5
Karpati, G.6
Carpenter, S.7
Watters, G.V.8
Wheeler, C.9
Witt, D.10
Bodell, A.11
Nelis, E.12
Van Broeckhoven, C.13
Lupski, J.R.14
-
18
-
-
0027337214
-
Mutation of the myelin Po gene in Charcot-Marie-Tooth neuropathy type 1
-
Hayasaka K., Ohnishi A., Takada G., Fukushima Y., Murai Y. Mutation of the myelin Po gene in Charcot-Marie-Tooth neuropathy type 1. Biochem Biophys Res Commun. 194:1993;1317-1322.
-
(1993)
Biochem Biophys Res Commun
, vol.194
, pp. 1317-1322
-
-
Hayasaka, K.1
Ohnishi, A.2
Takada, G.3
Fukushima, Y.4
Murai, Y.5
-
19
-
-
0018828556
-
The use of potassium ferricyanide in neural fixation
-
Langford L.A., Coggeshall R.E. The use of potassium ferricyanide in neural fixation. Anat Rec. 197:1980;297-303.
-
(1980)
Anat Rec
, vol.197
, pp. 297-303
-
-
Langford, L.A.1
Coggeshall, R.E.2
-
20
-
-
0016788436
-
Frequency of nerve fiber degeneration of peripheral motor and sensory neurons in amyotrophic lateral sclerosis - Morphometry of deep and superficial peroneal nerves
-
Dyck P.J., Stevens J.C., Mulder D.W., Espinosa R.E. Frequency of nerve fiber degeneration of peripheral motor and sensory neurons in amyotrophic lateral sclerosis - Morphometry of deep and superficial peroneal nerves. Neurology. 25:1975;781-785.
-
(1975)
Neurology
, vol.25
, pp. 781-785
-
-
Dyck, P.J.1
Stevens, J.C.2
Mulder, D.W.3
Espinosa, R.E.4
-
21
-
-
0018612391
-
De- And remyelination and onion bulb in cerebrotendinous xanthomatosis
-
Ohnishi A., Yamashita Y., Goto I., Kuroiwa Y., Murakami S., Ikeda M. De- and remyelination and onion bulb in cerebrotendinous xanthomatosis. Acta Neuropathol. 45:1979;43-45.
-
(1979)
Acta Neuropathol
, vol.45
, pp. 43-45
-
-
Ohnishi, A.1
Yamashita, Y.2
Goto, I.3
Kuroiwa, Y.4
Murakami, S.5
Ikeda, M.6
-
22
-
-
0021270968
-
Correlation between conduction studies and morphometric findings of sural nerve from eight normal volunteers
-
Nagaki J., Ohnishi A., Kuroiwa Y. Correlation between conduction studies and morphometric findings of sural nerve from eight normal volunteers. Clin Neurol (Tokyo). 24:1984;392-400.
-
(1984)
Clin Neurol (Tokyo)
, vol.24
, pp. 392-400
-
-
Nagaki, J.1
Ohnishi, A.2
Kuroiwa, Y.3
-
23
-
-
0024322088
-
Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding
-
Ohnishi A., Murai Y., Ikeda M., Fujita T., Furuya H., Kuroiwa Y. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding. Muscle Nerve. 12:1989;568-575.
-
(1989)
Muscle Nerve
, vol.12
, pp. 568-575
-
-
Ohnishi, A.1
Murai, Y.2
Ikeda, M.3
Fujita, T.4
Furuya, H.5
Kuroiwa, Y.6
-
24
-
-
0030728990
-
No evidence for axonal atrophy in human diabetic polyneuropathy
-
Engelstad J.N.K., Davies J.L., Giannini C., O'Brien P.C., Dyck P.J. No evidence for axonal atrophy in human diabetic polyneuropathy. J Neuropathol Exp Neurol. 56:1997;255-262.
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 255-262
-
-
Engelstad, J.N.K.1
Davies, J.L.2
Giannini, C.3
O'Brien, P.C.4
Dyck, P.J.5
-
25
-
-
0343889099
-
Morphological aspects of myelin and myelination
-
P. Morell. New York: Plenum Press
-
Raine C.S. Morphological aspects of myelin and myelination. Morell P. Myelin. 1984;1-49 Plenum Press, New York.
-
(1984)
Myelin
, pp. 1-49
-
-
Raine, C.S.1
-
26
-
-
0019519075
-
Permanent axotomy, a model of axonal atrophy and secondary segmental demyelination and remyelination
-
Dyck P.J., Lais A.C., Karnes J.L., Sparks M., Hunder H., Low P.A., Windebank A.J. Permanent axotomy, a model of axonal atrophy and secondary segmental demyelination and remyelination. Ann Neurol. 9:1981;575-583.
-
(1981)
Ann Neurol
, vol.9
, pp. 575-583
-
-
Dyck, P.J.1
Lais, A.C.2
Karnes, J.L.3
Sparks, M.4
Hunder, H.5
Low, P.A.6
Windebank, A.J.7
-
27
-
-
0021242286
-
The occurrence and significance of myelin with unusually large periodicity
-
King R.H.M., Thomas P.K. The occurrence and significance of myelin with unusually large periodicity. Acta Neuropathol. 63:1984;319-329.
-
(1984)
Acta Neuropathol
, vol.63
, pp. 319-329
-
-
King, R.H.M.1
Thomas, P.K.2
-
28
-
-
0025253083
-
Protein zero of peripheral nerve myelin: Biosynthesis, membrane insertion, and evidence of homotypic interaction
-
D'Urso D., Brophy P.J., Staugaitis S.M., Gillespie C.S., Frey A.B., Stempak J.G., Colman D.R. Protein zero of peripheral nerve myelin: biosynthesis, membrane insertion, and evidence of homotypic interaction. Neuron. 2:1990;449-460.
-
(1990)
Neuron
, vol.2
, pp. 449-460
-
-
D'Urso, D.1
Brophy, P.J.2
Staugaitis, S.M.3
Gillespie, C.S.4
Frey, A.B.5
Stempak, J.G.6
Colman, D.R.7
-
29
-
-
0025194356
-
Role of myelin Po protein as a homophilic adhesion molecule
-
Filbin M.T., Walsh F.S., Trapp B.D., Pizzey J.A., Tennekoon G.I. Role of myelin Po protein as a homophilic adhesion molecule. Nature. 344:1990;871-872.
-
(1990)
Nature
, vol.344
, pp. 871-872
-
-
Filbin, M.T.1
Walsh, F.S.2
Trapp, B.D.3
Pizzey, J.A.4
Tennekoon, G.I.5
-
30
-
-
0030246987
-
Crystal structure of the extracellular domain from Po, the major structural protein of peripheral nerve myelin
-
Shapiro L., Doyle J., Hensley P., Colman D.R., Hendrickson W.A. Crystal structure of the extracellular domain from Po, the major structural protein of peripheral nerve myelin. Neuron. 17:1996;435-449.
-
(1996)
Neuron
, vol.17
, pp. 435-449
-
-
Shapiro, L.1
Doyle, J.2
Hensley, P.3
Colman, D.R.4
Hendrickson, W.A.5
-
31
-
-
0024853861
-
Polyneuropathy associated with IgM monoclonal gammopathy: Immunological and pathological study of 31 patients
-
Vital A., Vital C., Julien J., Baquey A., Steck A.J. Polyneuropathy associated with IgM monoclonal gammopathy: immunological and pathological study of 31 patients. Acta Neuropathol. 79:1989;160-167.
-
(1989)
Acta Neuropathol
, vol.79
, pp. 160-167
-
-
Vital, A.1
Vital, C.2
Julien, J.3
Baquey, A.4
Steck, A.J.5
-
32
-
-
0028244197
-
The cytoplasmic domain of myelin glycoprotein Po interacts with negatively charged phospholipid bilayers
-
Ding Y., Brunden K.R. The cytoplasmic domain of myelin glycoprotein Po interacts with negatively charged phospholipid bilayers. J Biol Chem. 269:1994;10764-10770.
-
(1994)
J Biol Chem
, vol.269
, pp. 10764-10770
-
-
Ding, Y.1
Brunden, K.R.2
-
33
-
-
0029804244
-
Inherited demyelinating peripheral neuropathies: Relating myelin packing abnormalities to PO molecular defects
-
Kirshner D.A., Szumowski K., Gabreëls-Festen A.A.W.M., Hoogendijk J.E., Bolhuis P.A. Inherited demyelinating peripheral neuropathies: relating myelin packing abnormalities to PO molecular defects. J Neurosci Res. 46:1996;502-508.
-
(1996)
J Neurosci Res
, vol.46
, pp. 502-508
-
-
Kirshner, D.A.1
Szumowski, K.2
Gabreëls-Festen, A.A.W.M.3
Hoogendijk, J.E.4
Bolhuis, P.A.5
-
34
-
-
0019440524
-
Uncompacted myelin lamellae in dysglobulinemic neuropathy
-
Ohnishi A., Hirano A. Uncompacted myelin lamellae in dysglobulinemic neuropathy. J Neurol Sci. 51:1981;131-140.
-
(1981)
J Neurol Sci
, vol.51
, pp. 131-140
-
-
Ohnishi, A.1
Hirano, A.2
-
35
-
-
0028069302
-
Uncompacted myelin lamellae in polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome. Ultrastructural study of peripheral nerve biopsy from 22 patients
-
Vital C., Gherardi R., Vital A., Kopp N., Pellissier J.F., Soubrier M., Clavelou P., Bellance R., Delisle M.B., Ruchoux M.M., Hauw J.J. Uncompacted myelin lamellae in polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes syndrome. Ultrastructural study of peripheral nerve biopsy from 22 patients. Acta Neuropathol. 87:1994;302-307.
-
(1994)
Acta Neuropathol
, vol.87
, pp. 302-307
-
-
Vital, C.1
Gherardi, R.2
Vital, A.3
Kopp, N.4
Pellissier, J.F.5
Soubrier, M.6
Clavelou, P.7
Bellance, R.8
Delisle, M.B.9
Ruchoux, M.M.10
Hauw, J.J.11
-
36
-
-
0004085133
-
Schwann cells and myelin in the peripheral nervous system
-
Boston: Butterworth-Heinemann
-
Midroni G., Bilbao J.M. Schwann cells and myelin in the peripheral nervous system. Biopsy diagnosis of peripheral neuropathy. 1995;75-103 Butterworth-Heinemann, Boston.
-
(1995)
Biopsy Diagnosis of Peripheral Neuropathy
, pp. 75-103
-
-
Midroni, G.1
Bilbao, J.M.2
-
37
-
-
0025912158
-
Uncompacted inner myelin lamellae in inherited tendency to pressure palsy
-
Yoshikawa H., Dyck P.J. Uncompacted inner myelin lamellae in inherited tendency to pressure palsy. J Neuropathol Exp Neurol. 50:1991;649-657.
-
(1991)
J Neuropathol Exp Neurol
, vol.50
, pp. 649-657
-
-
Yoshikawa, H.1
Dyck, P.J.2
-
38
-
-
0027422165
-
De novo mutation of the myelin Po gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)
-
Hayasaka K., Himoro M., Sawaishi Y., Nanao K., Takahashi T., Takada G., Nicholson G.A., Ouvrier R.A., Tachi N. De novo mutation of the myelin Po gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Nat Genet. 5:1993;266-268.
-
(1993)
Nat Genet
, vol.5
, pp. 266-268
-
-
Hayasaka, K.1
Himoro, M.2
Sawaishi, Y.3
Nanao, K.4
Takahashi, T.5
Takada, G.6
Nicholson, G.A.7
Ouvrier, R.A.8
Tachi, N.9
-
39
-
-
0023127966
-
The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood
-
Ouvrier R.A., McLeod J.G., Conchin T.E. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood. Brain. 110:1987;121-148.
-
(1987)
Brain
, vol.110
, pp. 121-148
-
-
Ouvrier, R.A.1
McLeod, J.G.2
Conchin, T.E.3
-
40
-
-
0028824925
-
Protein zero (PO)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
-
Martini R., Zielasek J., Toyka K.V., Giese K.P., Schachner M. Protein zero (PO)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. Nat Genet. 11:1995;281-286.
-
(1995)
Nat Genet
, vol.11
, pp. 281-286
-
-
Martini, R.1
Zielasek, J.2
Toyka, K.V.3
Giese, K.P.4
Schachner, M.5
-
41
-
-
0030611992
-
Heterozygous Po knockout mice develop peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP)
-
Shy M.E., Arroyo E., Sladky J., Menichella D., Jiang H., Kamholz J., Scherer S.S. Heterozygous Po knockout mice develop peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). J Neuropathol Exp Neurol. 56:1997;811-821.
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 811-821
-
-
Shy, M.E.1
Arroyo, E.2
Sladky, J.3
Menichella, D.4
Jiang, H.5
Kamholz, J.6
Scherer, S.S.7
-
42
-
-
0028074645
-
Mutations in demyelinating peripheral neuropathies support the molecular model of myelin PO-glycoprotein extracellular domain
-
Kirschner D.A., Saavedra R.A. Mutations in demyelinating peripheral neuropathies support the molecular model of myelin PO-glycoprotein extracellular domain. J Neurosci Res. 39:1994;63-69.
-
(1994)
J Neurosci Res
, vol.39
, pp. 63-69
-
-
Kirschner, D.A.1
Saavedra, R.A.2
-
43
-
-
0030051641
-
High frequency mutations in codon 98 of the peripheral myelin protein Po gene in 20 French CMT 1 patients
-
Rouger H., Le Guern E., Gouider R., Tardieu S., Birouk N., Gugenheim M., Bouche P., Agid Y., Brice A. High frequency mutations in codon 98 of the peripheral myelin protein Po gene in 20 French CMT 1 patients. Am J Hum Genet. 58:1996;638-641.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 638-641
-
-
Rouger, H.1
Le Guern, E.2
Gouider, R.3
Tardieu, S.4
Birouk, N.5
Gugenheim, M.6
Bouche, P.7
Agid, Y.8
Brice, A.9
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