-
3
-
-
0036270792
-
Clinical manifestations and stages of Rett syndrome
-
Hagberg B: Clinical manifestations and stages of Rett syndrome. Ment Retard Dev Disabil Res Rev 2002;8:61-65.
-
(2002)
Ment Retard Dev Disabil Res Rev
, vol.8
, pp. 61-65
-
-
Hagberg, B.1
-
4
-
-
0141925713
-
DNA methylation and Rett syndrome
-
Kriaucionis S, Bird A: DNA methylation and Rett syndrome. Hum Mol Genet 2003;12(Suppl 2):R221-R227.
-
(2003)
Hum Mol Genet
, vol.12
, Issue.SUPPL. 2
-
-
Kriaucionis, S.1
Bird, A.2
-
5
-
-
0036917867
-
Rett syndrome and MECP2: Linking epigenetics and neuronal function
-
Shahbazian MD, Zoghbi HY: Rett syndrome and MECP2: Linking epigenetics and neuronal function. Am J Hum Genet 2002;71: 1259-1272.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1259-1272
-
-
Shahbazian, M.D.1
Zoghbi, H.Y.2
-
6
-
-
9244265544
-
Rett syndrome: Clinical and molecular update
-
Percy AK, Lane JB: Rett syndrome: Clinical and molecular update. Curr Opin Pediatr 2004;16:670-677.
-
(2004)
Curr Opin Pediatr
, vol.16
, pp. 670-677
-
-
Percy, A.K.1
Lane, J.B.2
-
7
-
-
0037215780
-
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2)
-
Moog U, Smeets EE, van Roozendaal KE, et al: Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2). Eur J Paediatr Neurol 2003;7:5-12.
-
(2003)
Eur J Paediatr Neurol
, vol.7
, pp. 5-12
-
-
Moog, U.1
Smeets, E.E.2
Van Roozendaal, K.E.3
-
8
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van den Veyver IB, Wan M, et al: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999;23:185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van Den Veyver, I.B.2
Wan, M.3
-
9
-
-
0026747761
-
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
-
Lewis JD, Meehan RR, Henzel WJ, et al: Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA. Cell 1992;69:905-914.
-
(1992)
Cell
, vol.69
, pp. 905-914
-
-
Lewis, J.D.1
Meehan, R.R.2
Henzel, W.J.3
-
10
-
-
0342437491
-
MECP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
-
Nan X, Campoy FJ, Bird A: MECP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell 1997;88:471-481.
-
(1997)
Cell
, vol.88
, pp. 471-481
-
-
Nan, X.1
Campoy, F.J.2
Bird, A.3
-
11
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
Chen RZ, Akbarian S, Tudor M, et al: Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet 2001;27:327-331.
-
(2001)
Nat Genet
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
-
12
-
-
0035094767
-
A mouse MECP2-null mutation causes neurological symptoms that mimic Rett syndrome
-
Guy J, Hendrich B, Holmes M, et al: A mouse MECP2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet 2001;27:322-326.
-
(2001)
Nat Genet
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
-
13
-
-
0037130455
-
Mice with truncated MECP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
-
Shahbazian M, Young J, Yuva-Paylor L, et al: Mice with truncated MECP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron 2002;35:243-254.
-
(2002)
Neuron
, vol.35
, pp. 243-254
-
-
Shahbazian, M.1
Young, J.2
Yuva-Paylor, L.3
-
14
-
-
12744261491
-
Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome
-
Moretti P, Bouwknecht JA, Teague R, et al: Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome. Hum Mol Genet 2005;14:205-220.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 205-220
-
-
Moretti, P.1
Bouwknecht, J.A.2
Teague, R.3
-
15
-
-
0037081840
-
Insight into Rett syndrome: MECP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
-
Shahbazian MD, Antalffy B, Armstrong DL, et al: Insight into Rett syndrome: MECP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Hum Mol Genet 2002;11:115-124.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 115-124
-
-
Shahbazian, M.D.1
Antalffy, B.2
Armstrong, D.L.3
-
16
-
-
0034007933
-
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions
-
Reichwald K, Thiesen J, Wiehe T, et al: Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions. Mamm Genome 2000;11:182-190.
-
(2000)
Mamm Genome
, vol.11
, pp. 182-190
-
-
Reichwald, K.1
Thiesen, J.2
Wiehe, T.3
-
17
-
-
0344232733
-
MicroRNAs: Runts of the genome assert themselves
-
Lai EC: MicroRNAs: Runts of the genome assert themselves. Curr Biol 2003;13:R925-R936.
-
(2003)
Curr Biol
, vol.13
-
-
Lai, E.C.1
-
18
-
-
0347444723
-
MicroRNAs: Genomics, biogenesis, mechanism, and function
-
Bartel DP: MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 2004;116:281-297.
-
(2004)
Cell
, vol.116
, pp. 281-297
-
-
Bartel, D.P.1
-
19
-
-
2542481314
-
The major form of MECP2 has a novel N-terminus generated by alternative splicing
-
Kriaucionis S, Bird A: The major form of MECP2 has a novel N-terminus generated by alternative splicing. Nucleic Acids Res 2004;32:1818-1823.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 1818-1823
-
-
Kriaucionis, S.1
Bird, A.2
-
20
-
-
12144287057
-
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
-
Mnatzakanian GN, Lohi H, Munteanu I, et al: A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. Nat Genet 2004;36:339-341.
-
(2004)
Nat Genet
, vol.36
, pp. 339-341
-
-
Mnatzakanian, G.N.1
Lohi, H.2
Munteanu, I.3
-
21
-
-
1942533500
-
Expression of MECP2 in postmitotic neurons rescues Rett syndrome in mice
-
Luikenhuis S, Giacometti E, Beard CF, et al: Expression of MECP2 in postmitotic neurons rescues Rett syndrome in mice. Proc Natl Acad Sci U S A 2004;101:6033-6038.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 6033-6038
-
-
Luikenhuis, S.1
Giacometti, E.2
Beard, C.F.3
-
22
-
-
8444253290
-
Mild overexpression of MECP2 causes a progressive neurological disorder in mice
-
Collins AL, Levenson JM, Vilaythong AP, et al: Mild overexpression of MECP2 causes a progressive neurological disorder in mice. Hum Mol Genet 2004;13:2679-2689.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2679-2689
-
-
Collins, A.L.1
Levenson, J.M.2
Vilaythong, A.P.3
-
23
-
-
1542270771
-
Expression of the methyl-CpG-binding protein MECP2 in rat brain. An ontogenetic study
-
Cassel S, Revel MO, Kelche C, et al: Expression of the methyl-CpG-binding protein MECP2 in rat brain. An ontogenetic study. Neurobiol Dis 2004;15:206-211.
-
(2004)
Neurobiol Dis
, vol.15
, pp. 206-211
-
-
Cassel, S.1
Revel, M.O.2
Kelche, C.3
-
24
-
-
0037396585
-
Expression of MECP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis
-
Cohen DR, Matarazzo V, Palmer AM, et al: Expression of MECP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis. Mol Cell Neurosci 2003;22:417-429.
-
(2003)
Mol Cell Neurosci
, vol.22
, pp. 417-429
-
-
Cohen, D.R.1
Matarazzo, V.2
Palmer, A.M.3
-
25
-
-
0032776138
-
A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3″-untranslated region of the methyl-CpG-binding protein 2 gene (MECP2) suggests a regulatory role in gene expression
-
Coy JF, Sedlacek Z, Bachner D, et al: A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3″-untranslated region of the methyl-CpG-binding protein 2 gene (MECP2) suggests a regulatory role in gene expression. Hum Mol Genet 1999;8:1253-1262.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1253-1262
-
-
Coy, J.F.1
Sedlacek, Z.2
Bachner, D.3
-
26
-
-
0037381336
-
The expression of methyl CpG binding factor MECP2 correlates with cellular differentiation in the developing rat brain and in cultured cells
-
Jung BP, Jugloff DG, Zhang G, et al: The expression of methyl CpG binding factor MECP2 correlates with cellular differentiation in the developing rat brain and in cultured cells. J Neurobiol 2003;55:86-96.
-
(2003)
J Neurobiol
, vol.55
, pp. 86-96
-
-
Jung, B.P.1
Jugloff, D.G.2
Zhang, G.3
-
27
-
-
7244243971
-
MECP2 is progressively expressed in postmigratory neurons and is involved in neuronal maturation rather than cell fate decisions
-
Kishi N, Macklis JD: MECP2 is progressively expressed in postmigratory neurons and is involved in neuronal maturation rather than cell fate decisions. Mol Cell Neurosci 2004;27:306-321.
-
(2004)
Mol Cell Neurosci
, vol.27
, pp. 306-321
-
-
Kishi, N.1
Macklis, J.D.2
-
28
-
-
1642441427
-
Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain
-
Mullaney BC, Johnston MV, Blue ME: Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain. Neuroscience 2004;123:939-949.
-
(2004)
Neuroscience
, vol.123
, pp. 939-949
-
-
Mullaney, B.C.1
Johnston, M.V.2
Blue, M.E.3
-
29
-
-
0037439239
-
Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: An immunochemical study of subcellular fractions
-
Aber KM, Nori P, MacDonald SM, et al: Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions. Neuroscience 2003;116:77-80.
-
(2003)
Neuroscience
, vol.116
, pp. 77-80
-
-
Aber, K.M.1
Nori, P.2
MacDonald, S.M.3
-
30
-
-
0042357071
-
Chromatin compaction by human MECP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation
-
Georgel PT, Horowitz-Scherer RA, Adkins N, et al: Chromatin compaction by human MECP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation. J Biol Chem 2003;278:32181-32188.
-
(2003)
J Biol Chem
, vol.278
, pp. 32181-32188
-
-
Georgel, P.T.1
Horowitz-Scherer, R.A.2
Adkins, N.3
-
31
-
-
0043178993
-
A mutant form of MECP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by Notch in Xenopus embryos
-
Stancheva I, Collins AL, Van den Veyver IB, et al: A mutant form of MECP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by Notch in Xenopus embryos. Mol Cell 2003;12:425-435.
-
(2003)
Mol Cell
, vol.12
, pp. 425-435
-
-
Stancheva, I.1
Collins, A.L.2
Van Den Veyver, I.B.3
-
32
-
-
0033617522
-
Notch signaling: Cell fate control and signal integration in development
-
Artavanis-Tsakonas S, Rand MD, Lake RJ: Notch signaling: cell fate control and signal integration in development. Science 1999;284:770-776.
-
(1999)
Science
, vol.284
, pp. 770-776
-
-
Artavanis-Tsakonas, S.1
Rand, M.D.2
Lake, R.J.3
-
33
-
-
0029977614
-
Mammalian hairy and Enhancer of split homolog 1 regulates differentiation of retinal neurons and is essential for eye morphogenesis
-
Tomita K, Ishibashi M, Nakahara K, et al: Mammalian hairy and Enhancer of split homolog 1 regulates differentiation of retinal neurons and is essential for eye morphogenesis. Neuron 1996;16:723-734.
-
(1996)
Neuron
, vol.16
, pp. 723-734
-
-
Tomita, K.1
Ishibashi, M.2
Nakahara, K.3
-
34
-
-
0028216808
-
Notch1 is essential for postimplantation development in mice
-
Swiatek PJ, Lindsell CE, del Amo FF, et al: Notch1 is essential for postimplantation development in mice. Genes Dev 1994;8:707-719.
-
(1994)
Genes Dev
, vol.8
, pp. 707-719
-
-
Swiatek, P.J.1
Lindsell, C.E.2
Del Amo, F.F.3
-
35
-
-
0028971681
-
Disruption of the mouse RBP-J kappa gene results in early embryonic death
-
Oka C, Nakano T, Wakeham A, et al: Disruption of the mouse RBP-J kappa gene results in early embryonic death. Development 1995;121:3291-3301.
-
(1995)
Development
, vol.121
, pp. 3291-3301
-
-
Oka, C.1
Nakano, T.2
Wakeham, A.3
-
36
-
-
0028989016
-
Notch1 is required for the coordinate segmentation of somites
-
Conlon RA, Reaume AG, Rossant J: Notch1 is required for the coordinate segmentation of somites. Development 1995;121:1533-1545.
-
(1995)
Development
, vol.121
, pp. 1533-1545
-
-
Conlon, R.A.1
Reaume, A.G.2
Rossant, J.3
-
37
-
-
0037636512
-
Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function
-
Zhao X, Ueba T, Christie BR, et al: Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function. Proc Natl Acad Sci U S A 2003;100:6777-6782.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 6777-6782
-
-
Zhao, X.1
Ueba, T.2
Christie, B.R.3
-
38
-
-
0242332183
-
Depression of BDNF transcription involves calcium-dependent phosphorylation of MECP2
-
Chen WG, Chang Q, Lin Y, et al: Depression of BDNF transcription involves calcium-dependent phosphorylation of MECP2. Science 2003;302:885-889.
-
(2003)
Science
, vol.302
, pp. 885-889
-
-
Chen, W.G.1
Chang, Q.2
Lin, Y.3
-
39
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
Horike S, Cai S, Miyano M, et al: Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat Genet 2005;37:31-40.
-
(2005)
Nat Genet
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
-
40
-
-
0242300612
-
DNA-methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
-
Martinowich K, Hattori D, Wu H, et al: DNA-methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science 2003;302:890-893.
-
(2003)
Science
, vol.302
, pp. 890-893
-
-
Martinowich, K.1
Hattori, D.2
Wu, H.3
-
41
-
-
4444333589
-
The transcriptional repressor MECP2 regulates terminal neuronal differentiation
-
Matarazzo V, Cohen D, Palmer AM, et al: The transcriptional repressor MECP2 regulates terminal neuronal differentiation. Mol Cell Neurosci 2004;27:44-58.
-
(2004)
Mol Cell Neurosci
, vol.27
, pp. 44-58
-
-
Matarazzo, V.1
Cohen, D.2
Palmer, A.M.3
-
42
-
-
0028904853
-
Selective dendritic alterations in the cortex of Rett syndrome
-
Armstrong D, Dunn JK, Antalffy B, et al: Selective dendritic alterations in the cortex of Rett syndrome. J Neuropathol Exp Neurol 1995;54:195-201.
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 195-201
-
-
Armstrong, D.1
Dunn, J.K.2
Antalffy, B.3
-
43
-
-
0029059624
-
Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome
-
Bauman ML, Kemper TL, Arin DM: Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome. Neurology 1995;45:1581-1586.
-
(1995)
Neurology
, vol.45
, pp. 1581-1586
-
-
Bauman, M.L.1
Kemper, T.L.2
Arin, D.M.3
-
44
-
-
0029062591
-
Microscopic observations of the brain in Rett syndrome
-
Bauman ML, Kemper TL, Arin DM: Microscopic observations of the brain in Rett syndrome. Neuropediatrics 1995;26:105-108.
-
(1995)
Neuropediatrics
, vol.26
, pp. 105-108
-
-
Bauman, M.L.1
Kemper, T.L.2
Arin, D.M.3
-
45
-
-
0042133327
-
Brain-derived neurotrophic factor is required for the maintenance of cortical dendrites
-
Gorski JA, Zeiler SR, Tamowski S, et al: Brain-derived neurotrophic factor is required for the maintenance of cortical dendrites. J Neurosci 2003;23:6856-6865.
-
(2003)
J Neurosci
, vol.23
, pp. 6856-6865
-
-
Gorski, J.A.1
Zeiler, S.R.2
Tamowski, S.3
-
46
-
-
0033710349
-
Cortical degeneration in the absence of neurotrophin signaling: Dendritic retraction and neuronal loss after removal of the receptor TrkB
-
Xu B, Zang K, Ruff NL, et al: Cortical degeneration in the absence of neurotrophin signaling: Dendritic retraction and neuronal loss after removal of the receptor TrkB. Neuron 2000;26:233-245.
-
(2000)
Neuron
, vol.26
, pp. 233-245
-
-
Xu, B.1
Zang, K.2
Ruff, N.L.3
-
47
-
-
0034043146
-
Neocortical neurons lacking the protein-tyrosine kinase B receptor display abnormal differentiation and process elongation in vitro and in vivo
-
Gates MA, Tai CC, Macklis JD: Neocortical neurons lacking the protein-tyrosine kinase B receptor display abnormal differentiation and process elongation in vitro and in vivo. Neuroscience 2000;98:437-447.
-
(2000)
Neuroscience
, vol.98
, pp. 437-447
-
-
Gates, M.A.1
Tai, C.C.2
Macklis, J.D.3
-
48
-
-
0029135317
-
Reduced size of corpus callosum in autism
-
Egaas B, Courchesne E, Saitoh O: Reduced size of corpus callosum in autism. Arch Neurol 1995;52:794-801.
-
(1995)
Arch Neurol
, vol.52
, pp. 794-801
-
-
Egaas, B.1
Courchesne, E.2
Saitoh, O.3
-
49
-
-
0035192560
-
Magnetic resonance imaging and clinical findings examined in adulthood-Studies on three adults with Rett syndrome
-
Gotoh H, Suzuki I, Maruki K, et al: Magnetic resonance imaging and clinical findings examined in adulthood-Studies on three adults with Rett syndrome. Brain Dev 2001;23(Suppl 1):S118-S121.
-
(2001)
Brain Dev
, vol.23
, Issue.SUPPL. 1
-
-
Gotoh, H.1
Suzuki, I.2
Maruki, K.3
-
50
-
-
0034069651
-
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
-
Escayg A, MacDonald BT, Meisler MH, et al: Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet 2000;24:343-345.
-
(2000)
Nat Genet
, vol.24
, pp. 343-345
-
-
Escayg, A.1
MacDonald, B.T.2
Meisler, M.H.3
-
51
-
-
17344367657
-
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B
-
Wallace RH, Wang DW, Singh R, et al: Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B. Nat Genet 1998;19:366-370.
-
(1998)
Nat Genet
, vol.19
, pp. 366-370
-
-
Wallace, R.H.1
Wang, D.W.2
Singh, R.3
-
52
-
-
18744405062
-
Corepressor-dependent silencing of chromosomal regions encoding neuronal genes
-
Lunyak VV, Burgess R, Prefontaine GG, et al: Corepressor-dependent silencing of chromosomal regions encoding neuronal genes. Science 2002;298:1747-1752.
-
(2002)
Science
, vol.298
, pp. 1747-1752
-
-
Lunyak, V.V.1
Burgess, R.2
Prefontaine, G.G.3
-
53
-
-
0034131122
-
Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice
-
Planells-Cases R, Caprini M, Zhang J, et al: Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice. Biophys J 2000;78:2878-2891.
-
(2000)
Biophys J
, vol.78
, pp. 2878-2891
-
-
Planells-Cases, R.1
Caprini, M.2
Zhang, J.3
-
54
-
-
0036337338
-
Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression
-
Stuhmer T, Anderson SA, Ekker M, et al: Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression. Development 2002;129:245-252.
-
(2002)
Development
, vol.129
, pp. 245-252
-
-
Stuhmer, T.1
Anderson, S.A.2
Ekker, M.3
-
55
-
-
0032830639
-
Rett syndome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van den Veyver IV, Wan M, et al: Rett syndome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics 1999;23(2):127-128.
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 127-128
-
-
Amir, R.E.1
Van Veyver IV, D.2
Wan, M.3
-
56
-
-
0014011176
-
Uber ein zerebral-atrophisches syndrome bei hyperammonemie
-
Rett A: Uber ein zerebral-atrophisches Syndrome bei Hyperammonemie. Wien Med Wochenschr 1966;116:723-726.
-
(1966)
Wien Med Wochenschr
, vol.116
, pp. 723-726
-
-
Rett, A.1
|