-
1
-
-
0015464659
-
Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects
-
Behse F, Buchthal F, Carlsen F, Knappeis GG (1972) Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects. Brain 95:777-794
-
(1972)
Brain
, vol.95
, pp. 777-794
-
-
Behse, F.1
Buchthal, F.2
Carlsen, F.3
Knappeis, G.G.4
-
2
-
-
0019956792
-
A comparison of early morphological changes at denervated and paralyzed end-plates in fast and slow muscles in the mouse
-
Brown MC, Hopkins WG, Keynes RJ, White I (1982) A comparison of early morphological changes at denervated and paralyzed end-plates in fast and slow muscles in the mouse. Brain Res 248:382-286
-
(1982)
Brain Res.
, vol.248
, pp. 382-386
-
-
Brown, M.C.1
Hopkins, W.G.2
Keynes, R.J.3
White, I.4
-
3
-
-
0018120729
-
Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease
-
Carpenter S, Karpati G, Rothman S, Watters G, Andermann F (1978) Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease. Acta Neuropathol (Berl) 42:91-97
-
(1978)
Acta Neuropathol. (Berl.)
, vol.42
, pp. 91-97
-
-
Carpenter, S.1
Karpati, G.2
Rothman, S.3
Watters, G.4
Andermann, F.5
-
4
-
-
0000494564
-
The significance of the "dying-back" process in experimental and human neurological disease
-
Cavanagh JB (1964) The significance of the "dying-back" process in experimental and human neurological disease. Int Rev Exp Pathol 3:219-267
-
(1964)
Int. Rev. Exp. Pathol.
, vol.3
, pp. 219-267
-
-
Cavanagh, J.B.1
-
5
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD (1993) DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72:143-151
-
(1993)
Cell
, vol.72
, pp. 143-151
-
-
Chance, P.F.1
Alderson, M.K.2
Leppig, K.A.3
Lensch, M.W.4
Matsunami, N.5
Smith, B.6
Swanson, P.D.7
Odelberg, S.J.8
Disteche, C.M.9
Bird, T.D.10
-
6
-
-
0024401106
-
Peripheral nerve involvement in Werdnig-Hoffmann disease
-
Chien YY, Nonaka I (1989) Peripheral nerve involvement in Werdnig-Hoffmann disease. Brain Dev 11:221-229
-
(1989)
Brain Dev.
, vol.11
, pp. 221-229
-
-
Chien, Y.Y.1
Nonaka, I.2
-
7
-
-
71749091926
-
Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model
-
Cifuentes-Diaz C, Nicole S, Velasco ME, Borra-Cebrian C, Panozzo C, Frugier T, Millet G, Roblot N, Joshi V, Melki J (2002) Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model. Hum Mol Genet 11:1439-1447
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1439-1447
-
-
Cifuentes-Diaz, C.1
Nicole, S.2
Velasco, M.E.3
Borra-Cebrian, C.4
Panozzo, C.5
Frugier, T.6
Millet, G.7
Roblot, N.8
Joshi, V.9
Melki, J.10
-
8
-
-
0029257498
-
Neuromuscular degeneration (nmd): A mutation on mouse chromosome 19 that causes motor neuron degeneration
-
Cook SA, Johnson KR, Bronson RT, Davisson MT (1995) Neuromuscular degeneration (nmd): A mutation on mouse chromosome 19 that causes motor neuron degeneration. Mamm Genome 6:187-191
-
(1995)
Mamm. Genome
, vol.6
, pp. 187-191
-
-
Cook, S.A.1
Johnson, K.R.2
Bronson, R.T.3
Davisson, M.T.4
-
9
-
-
0032408306
-
Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele
-
Cox GA, Mahaffey CL, Frankel WN (1998) Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron 21:1327-1337
-
(1998)
Neuron.
, vol.21
, pp. 1327-1337
-
-
Cox, G.A.1
Mahaffey, C.L.2
Frankel, W.N.3
-
10
-
-
0018895282
-
Human ontogenesis. II. Development of the human neuromuscular junction
-
Fidzianska A (1980) Human ontogenesis. II. Development of the human neuromuscular junction. J Neuropathol Exp Neurol 39:606-615
-
(1980)
J. Neuropathol. Exp. Neurol.
, vol.39
, pp. 606-615
-
-
Fidzianska, A.1
-
11
-
-
0025215242
-
Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism
-
Fidzianska A, Goebel HH, Warlo I (1990) Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism. Brain 113:433-445
-
(1990)
Brain
, vol.113
, pp. 433-445
-
-
Fidzianska, A.1
Goebel, H.H.2
Warlo, I.3
-
12
-
-
0032940401
-
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33
-
Gabreëls-Festen A, Beersum S van, Eshuis L, LeGuern E, Gabreels F, Engelen B van, Mariman E (1999) Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33. J Neurol Neurosurg Psychiatry 66:569-574.
-
(1999)
J. Neurol. Neurosurg. Psychiatry
, vol.66
, pp. 569-574
-
-
Gabreëls-Festen, A.1
van Beersum, S.2
Eshuis, L.3
LeGuern, E.4
Gabreels, F.5
van Engelen, B.6
Mariman, E.7
-
13
-
-
0019925158
-
Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life
-
Guzzetta F, Ferriere G, Lyon G (1982) Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life. Brain 105:395-416
-
(1982)
Brain
, vol.105
, pp. 395-416
-
-
Guzzetta, F.1
Ferriere, G.2
Lyon, G.3
-
14
-
-
0033358195
-
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form is linked to chromosome 11q13-q21
-
Grohmann K. Wienker T.F. Saar K. Rudnik-Schoneborn S. Stoltenburg-Didinger G. Rossi R. Novelli G. Nürnberg G. Pfeufer A. Wirth B. et al. (1999) Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form is linked to chromosome 11q13-q21. Am J Hum Genet 65:1459-1462
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1459-1462
-
-
Grohmann, K.1
Wienker, T.F.2
Saar, K.3
Rudnik-Schoneborn, S.4
Stoltenburg-Didinger, G.5
Rossi, R.6
Novelli, G.7
Nürnberg, G.8
Pfeufer, A.9
Wirth, B.10
-
15
-
-
17944374029
-
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
-
Grohmann K, Schuelke M, Diers A, Hoffmann K, Lucke B, Adams C, Bertini E, Leonhardt-Horti H, Muntoni F, Ouvrier R, et al (2001) Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. Nat Genet 29:75-77
-
(2001)
Nat. Genet.
, vol.29
, pp. 75-77
-
-
Grohmann, K.1
Schuelke, M.2
Diers, A.3
Hoffmann, K.4
Lucke, B.5
Adams, C.6
Bertini, E.7
Leonhardt-Horti, H.8
Muntoni, F.9
Ouvrier, R.10
-
16
-
-
10744222932
-
Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)
-
Grohmann K, Varon R, Stolz P, Schuelke M, Janetzki C, Bertini E, Bushby K, Muntoni F, Ouvrier R, Van Maldergem L, et al (2003) Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1). Ann Neurol 54:719-724
-
(2003)
Ann. Neurol.
, vol.54
, pp. 719-724
-
-
Grohmann, K.1
Varon, R.2
Stolz, P.3
Schuelke, M.4
Janetzki, C.5
Bertini, E.6
Bushby, K.7
Muntoni, F.8
Ouvrier, R.9
Van Maldergem, L.10
-
17
-
-
5744242172
-
Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)
-
Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M (2004) Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1). Hum Mol Genet 13:2031-2042
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2031-2042
-
-
Grohmann, K.1
Rossoll, W.2
Kobsar, I.3
Holtmann, B.4
Jablonka, S.5
Wessig, C.6
Stoltenburg-Didinger, G.7
Fischer, U.8
Hübner, C.9
Martini, R.10
Sendtner, M.11
-
18
-
-
0027221141
-
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
-
Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, Bird TD, Conneally PM, Chance PF (1993) Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat Genet 5:31-34
-
(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.D.7
Conneally, P.M.8
Chance, P.F.9
-
19
-
-
0022368276
-
Qualitative and quantitative morphology of human sural nerve at different ages
-
Jacobs JM, Love S (1985) Qualitative and quantitative morphology of human sural nerve at different ages. Brain 108:897-924
-
(1985)
Brain
, vol.108
, pp. 897-924
-
-
Jacobs, J.M.1
Love, S.2
-
20
-
-
0030750954
-
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region
-
Korinthenberg R, Sauer M, Ketelsen UP, Hanemann CO, Stoll G, Graf M, Baborie A, Volk B, Wirth B, Rudnik-Schöneborn S, Zerres K (1997) Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region. Ann Neurol 42:364-368
-
(1997)
Ann. Neurol.
, vol.42
, pp. 364-368
-
-
Korinthenberg, R.1
Sauer, M.2
Ketelsen, U.P.3
Hanemann, C.O.4
Stoll, G.5
Graf, M.6
Baborie, A.7
Volk, B.8
Wirth, B.9
Rudnik-Schöneborn, S.10
Zerres, K.11
-
21
-
-
2942709863
-
Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathy
-
Maddatu TP, Garvey SM, Schroeder DG, HamptonTG, Cox GA (2004) Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathy. Hum Mol Genet 13:1105-1115
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1105-1115
-
-
Maddatu, T.P.1
Garvey, S.M.2
Schroeder, D.G.3
Hampton, T.G.4
Cox, G.A.5
-
22
-
-
0000325399
-
The pathology of neuropathies with focal thickening of the myelin sheath (tomaculous neuropathy). Studies on the formation of the abnormal myelin sheath
-
Madrid R, Bradley WG (1975) The pathology of neuropathies with focal thickening of the myelin sheath (tomaculous neuropathy). Studies on the formation of the abnormal myelin sheath. J Neurol Sci 25:415-448
-
(1975)
J. Neurol. Sci.
, vol.25
, pp. 415-448
-
-
Madrid, R.1
Bradley, W.G.2
-
23
-
-
0036842251
-
A missense mutation in Tbce causes progressive motor neuronopathy in mice
-
Martin N, Jaubert J, Gounon P, Salido E, Haase G, Szatanik M, Guenet JL (2002) A missense mutation in Tbce causes progressive motor neuronopathy in mice. Nat Genet 32:443-447
-
(2002)
Nat. Genet.
, vol.32
, pp. 443-447
-
-
Martin, N.1
Jaubert, J.2
Gounon, P.3
Salido, E.4
Haase, G.5
Szatanik, M.6
Guenet, J.L.7
-
24
-
-
0015296378
-
Acetylcholinesterase activity in suction biopsies of the rectum in the diagnosis of Hirschsprung's disease
-
Meier-Ruge W, Lutterbeck PM, Herzog B, Morger R, Moser R Schärli A (1972) Acetylcholinesterase activity in suction biopsies of the rectum in the diagnosis of Hirschsprung's disease. J Pediatr Surg 7:11-17
-
(1972)
J. Pediatr. Surg.
, vol.7
, pp. 11-17
-
-
Meier-Ruge, W.1
Lutterbeck, P.M.2
Herzog, B.3
Morger, R.4
Moser, R.5
Schärli, A.6
-
25
-
-
0014431636
-
Electrophysiology and electron microscopy of rat neuromuscular junctions after denervation
-
Miledi R, Slater CR (1968) Electrophysiology and electron microscopy of rat neuromuscular junctions after denervation. Proc R Soc Lond B Biol Sci 69:289-306
-
(1968)
Proc. R. Soc. Lond. B Biol. Sci.
, vol.169
, pp. 289-306
-
-
Miledi, R.1
Slater, C.R.2
-
26
-
-
0035030358
-
Inherited early onset severe axonal polyneuropathy with respiratory failure and autonomic involvement
-
Mohan U, Misra VP, Britto J, Muntoni F, King RH, Thomas P (2001) Inherited early onset severe axonal polyneuropathy with respiratory failure and autonomic involvement. Neuromuscul Disord 11:395-399
-
(2001)
Neuromuscul. Disord.
, vol.11
, pp. 395-399
-
-
Mohan, U.1
Misra, V.P.2
Britto, J.3
Muntoni, F.4
King, R.H.5
Thomas, P.6
-
27
-
-
0033554290
-
The "CMT rat": Peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22
-
Niemann S, Sereda MW, Rossner M, Stewart H, Suter U, Meinck HM, Griffiths IR, Nave KA (1999) The "CMT rat": Peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22. Ann N Y Acad Sci 883:254-261
-
(1999)
Ann. N. Y. Acad. Sci.
, vol.883
, pp. 254-261
-
-
Niemann, S.1
Sereda, M.W.2
Rossner, M.3
Stewart, H.4
Suter, U.5
Meinck, H.M.6
Griffiths, I.R.7
Nave, K.A.8
-
28
-
-
0021709735
-
Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases
-
Nordborg C, Conradi N, Sourander P, Hagberg B, Westerberg B (1984) Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases. Acta Neuropathol (Berl) 65:1-9
-
(1984)
Acta Neuropathol. (Berl.)
, vol.65
, pp. 1-9
-
-
Nordborg, C.1
Conradi, N.2
Sourander, P.3
Hagberg, B.4
Westerberg, B.5
-
29
-
-
0031868502
-
Axonal neuropathy and predominance of type II myofibres in infantile spinal muscular atrophy
-
Omran H, Ketelsen UP, Heinen F, Sauer M, Rudnik-Schöneborn S, Wirth B, Zerres K, Kratzer W, Korinthenberg R (1998) Axonal neuropathy and predominance of type II myofibres in infantile spinal muscular atrophy. J Child Neurol 13:327-331
-
(1998)
J. Child Neurol.
, vol.13
, pp. 327-331
-
-
Omran, H.1
Ketelsen, U.P.2
Heinen, F.3
Sauer, M.4
Rudnik-Schöneborn, S.5
Wirth, B.6
Zerres, K.7
Kratzer, W.8
Korinthenberg, R.9
-
31
-
-
0345306176
-
Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1
-
Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R (2003) Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. Brain 126:2682-2692
-
(2003)
Brain
, vol.126
, pp. 2682-2692
-
-
Pitt, M.1
Houlden, H.2
Jacobs, J.3
Mok, Q.4
Harding, B.5
Reilly, M.6
Surtees, R.7
-
32
-
-
9344241377
-
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
-
Quattrone A. Gambardella A. Bono F. Aguglia U. Bolino A. Bruni A.C. Montesi M.P. Oliveri R.L. Sabatelli M. Tamburrini O. et al. (1996) Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family. Neurology 46:1318-1324
-
(1996)
Neurology
, vol.46
, pp. 1318-1324
-
-
Quattrone, A.1
Gambardella, A.2
Bono, F.3
Aguglia, U.4
Bolino, A.5
Bruni, A.C.6
Montesi, M.P.7
Oliveri, R.L.8
Sabatelli, M.9
Tamburrini, O.10
-
33
-
-
0033782833
-
Classification of the hereditary motor and sensory neuropathies
-
Reilly MM (2000) Classification of the hereditary motor and sensory neuropathies. Curr Opin Neurol 13:561-564
-
(2000)
Curr. Opin. Neurol.
, vol.13
, pp. 561-564
-
-
Reilly, M.M.1
-
34
-
-
84907126089
-
Embedding in epoxy resins for ultra-thin sections in electron microscopy
-
Richardson KC, Janett L, Finke EH (1960) Embedding in epoxy resins for ultra-thin sections in electron microscopy. Stain Technol 35:313-323
-
(1960)
Stain. Technol.
, vol.35
, pp. 313-323
-
-
Richardson, K.C.1
Janett, L.2
Finke, E.H.3
-
35
-
-
0037465776
-
Classic infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy
-
Rudnik-Schöneborn S, Goebel HH, Schlote W, Molaian S, Omran H, Ketelsen U, Korinthenberg R, Wenzel D, Lauffer H, Kreiss-Nachtsheim M, et al (2003) Classic infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy. Neurology 60:983-987
-
(2003)
Neurology
, vol.60
, pp. 983-987
-
-
Rudnik-Schöneborn, S.1
Goebel, H.H.2
Schlote, W.3
Molaian, S.4
Omran, H.5
Ketelsen, U.6
Korinthenberg, R.7
Wenzel, D.8
Lauffer, H.9
Kreiss-Nachtsheim, M.10
-
36
-
-
0035511932
-
Induction, assembly, maturation and maintenance of a postsynaptic apparatus
-
Sanes JR, Lichtman JW (2001) Induction, assembly, maturation and maintenance of a postsynaptic apparatus. Nat Rev Neurosci 2:791-805
-
(2001)
Nat. Rev. Neurosci.
, vol.2
, pp. 791-805
-
-
Sanes, J.R.1
Lichtman, J.W.2
-
37
-
-
0024367577
-
Families of neural adhesion molecules
-
Schachner M (1989) Families of neural adhesion molecules. Ciba Found Symp 145:156-169
-
(1989)
Ciba Found. Symp.
, vol.145
, pp. 156-169
-
-
Schachner, M.1
-
38
-
-
0023774277
-
Changes of the ratio between myelin thickness and axon diameter in human developing sural, femoral, ulnar, facial, and trochlear nerves
-
Schröer JM, Bohl J, Bardeleben U von (1988) Changes of the ratio between myelin thickness and axon diameter in human developing sural, femoral, ulnar, facial, and trochlear nerves. Acta Neuropathol 76:471-483
-
(1988)
Acta Neuropathol.
, vol.76
, pp. 471-483
-
-
Schröder, J.M.1
Bohl, J.2
von Bardeleben, U.3
-
39
-
-
26444560429
-
Minimale Muskelfaserkaliber bei neurogenen Muskelatrophien
-
Doctoral Thesis. Universität Mainz
-
Seeger M (1979) Minimale Muskelfaserkaliber bei neurogenen Muskelatrophien. Doctoral Thesis. Universität Mainz
-
(1979)
-
-
Seeger, M.1
-
40
-
-
0343930751
-
Schwann cells induce and guide sprouting and reinnervation of neuromuscular junctions
-
Son YJ, Trachtenberg JT, Thompson WJ (1996) Schwann cells induce and guide sprouting and reinnervation of neuromuscular junctions. Science 19:280-285
-
(1996)
Science
, vol.19
, pp. 280-285
-
-
Son, Y.J.1
Trachtenberg, J.T.2
Thompson, W.J.3
-
41
-
-
0017341966
-
Ultrastructural studies of the dying-back process. III. The evolution of experimental peripheral giant axonal degeneration
-
Spencer PS, Schaumburg HH (1977) Ultrastructural studies of the dying-back process. III. The evolution of experimental peripheral giant axonal degeneration. J Neuropathol Exp Neurol 36:276-299
-
(1977)
J. Neuropathol. Exp. Neurol.
, vol.36
, pp. 276-299
-
-
Spencer, P.S.1
Schaumburg, H.H.2
-
42
-
-
0028079552
-
Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome
-
Thomas FP, Lebo RV, Rosoklija G, Ding XS, Lovelace RE, Latov N, Hays AP (1994) Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome. Acta Neuropathol 87:91-97
-
(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
-
43
-
-
0023194132
-
Congenital hypo- and hypermyelination neuropathy. Two cases
-
Vallat JM, Gil R, Leboutet MJ, Hugon J, Moulies D (1987) Congenital hypo- and hypermyelination neuropathy. Two cases. Acta Neuropathol (Berl) 74:197-201
-
(1987)
Acta Neuropathol. (Berl.)
, vol.74
, pp. 197-201
-
-
Vallat, J.M.1
Gil, R.2
Leboutet, M.J.3
Hugon, J.4
Moulies, D.5
-
44
-
-
9344241377
-
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
-
Quattrone A. Gambardella A. Bono F. Aguglia U. Bolino A. Bruni A.C. Montesi M.P. Oliveri R.L. Sabatelli M. Tamburrini O. et al. (1996) Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family. Neurology 46:1318-1324
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(1996)
Neurology
, vol.46
, pp. 1318-1324
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Quattrone, A.1
Gambardella, A.2
Bono, F.3
Aguglia, U.4
Bolino, A.5
Bruni, A.C.6
Montesi, M.P.7
Oliveri, R.L.8
Sabatelli, M.9
Tamburrini, O.10
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