-
1
-
-
23644439777
-
Proposed definition and classification of cerebral palsy
-
Bax M, Goldstein M, Rosenbaum P, Leviton A, Paneth N, Dan B, Jacobsson B, Damiano D (2005) Proposed definition and classification of cerebral palsy. Dev Med Child Neurol 47(8):571-576
-
(2005)
Dev Med Child Neurol
, vol.47
, Issue.8
, pp. 571-576
-
-
Bax, M.1
Goldstein, M.2
Rosenbaum, P.3
Leviton, A.4
Paneth, N.5
Dan, B.6
Jacobsson, B.7
Damiano, D.8
-
2
-
-
84868622976
-
Clinical prognostic messages from a systematic review on cerebral palsy
-
Novak I, Hines M, Goldsmith S, Barclay R (2012) Clinical prognostic messages from a systematic review on cerebral palsy. Pediatrics 130(5):e1285-e1312
-
(2012)
Pediatrics
, vol.130
, Issue.5
-
-
Novak, I.1
Hines, M.2
Goldsmith, S.3
Barclay, R.4
-
4
-
-
0034087090
-
Cerebral palsy and multiple births in China
-
Liu J, Li Z, Lin Q, Zhao P, Zhao F, Hong S, Li S (2000) Cerebral palsy and multiple births in China. Int J Epidemiol 29(2):292-299
-
(2000)
Int J Epidemiol
, vol.29
, Issue.2
, pp. 292-299
-
-
Liu, J.1
Li, Z.2
Lin, Q.3
Zhao, P.4
Zhao, F.5
Hong, S.6
Li, S.7
-
5
-
-
40649093087
-
Genetics considerations in cerebral palsy
-
Schaefer GB (2008) Genetics considerations in cerebral palsy. Semin Pediatr Neurol 15(1):21-26
-
(2008)
Semin Pediatr Neurol
, vol.15
, Issue.1
, pp. 21-26
-
-
Schaefer, G.B.1
-
6
-
-
61449562175
-
Causative factors in cerebral palsy
-
Nelson KB (2008) Causative factors in cerebral palsy. Clin Obstet Gynecol 51(4):749-762
-
(2008)
Clin Obstet Gynecol
, vol.51
, Issue.4
, pp. 749-762
-
-
Nelson, K.B.1
-
7
-
-
84857058937
-
Genetic insights into the causes and classification of the cerebral palsies
-
Moreno-De-Luca A, Ledbetter DH, Martin CL (2012) Genetic insights into the causes and classification of the cerebral palsies. Lancet Neurol 11(3):283-292
-
(2012)
Lancet Neurol
, vol.11
, Issue.3
, pp. 283-292
-
-
Moreno-De-Luca, A.1
Ledbetter, D.H.2
Martin, C.L.3
-
8
-
-
39749202947
-
Cerebral palsy and congenital malformations
-
Garne E, Dolk H, Krageloh-Mann I, Ravn SH, Cans C, Grp SC (2008) Cerebral palsy and congenital malformations. Eur J Pae-diatr Neurol 12(2):82-88
-
(2008)
Eur J Pae-diatr Neurol
, vol.12
, Issue.2
, pp. 82-88
-
-
Garne, E.1
Dolk, H.2
Krageloh-Mann, I.3
Ravn, S.H.4
Cans, C.5
Grp, S.C.6
-
9
-
-
33947593369
-
Is cerebral palsy associated with birth defects other than cerebral defects?
-
Blair E, Al Asedy F, Badawi N, Bower C (2007) Is cerebral palsy associated with birth defects other than cerebral defects? Dev Med Child Neurol 49(4):252-258
-
(2007)
Dev Med Child Neurol
, vol.49
, Issue.4
, pp. 252-258
-
-
Blair, E.1
Al Asedy, F.2
Badawi, N.3
Bower, C.4
-
10
-
-
34247161412
-
High familial risks for cerebral palsy implicate partial heritable aetiology
-
Hemminki K, Li X, Sundquist K, Sundquist J (2007) High familial risks for cerebral palsy implicate partial heritable aetiology. Paediatr Perinat Epidemiol 21(3):235-241
-
(2007)
Paediatr Perinat Epidemiol
, vol.21
, Issue.3
, pp. 235-241
-
-
Hemminki, K.1
Li, X.2
Sundquist, K.3
Sundquist, J.4
-
11
-
-
0014548720
-
Identical syndromes of cerebral palsy in the same family
-
Gustavson KH, Hagberg B, Sanner G (1969) Identical syndromes of cerebral palsy in the same family. Acta Paediatr Scand 58(4):330-340
-
(1969)
Acta Paediatr Scand
, vol.58
, Issue.4
, pp. 330-340
-
-
Gustavson, K.H.1
Hagberg, B.2
Sanner, G.3
-
12
-
-
6444242582
-
Estimated frequency of genetic and nongenetic causes of congenital idiopathic cerebral palsy in west Sweden
-
Costeff H (2004) Estimated frequency of genetic and nongenetic causes of congenital idiopathic cerebral palsy in west Sweden. Ann Hum Genet 68:515-520
-
(2004)
Ann Hum Genet
, vol.68
, pp. 515-520
-
-
Costeff, H.1
-
13
-
-
0034035450
-
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12
-
McHale DP, Jackson AP, Campbell Levene MI, Corry P, Woods CG, Lench NJ, Mueller RF, Markham AF (2000) A gene for ataxic cerebral palsy maps to chromosome 9p12-q12. Eur J Hum Genet 8(4):267-272
-
(2000)
Eur J Hum Genet
, vol.8
, Issue.4
, pp. 267-272
-
-
McHale, D.P.1
Jackson, A.P.2
Campbell Levene, M.I.3
Corry, P.4
Woods, C.G.5
Lench, N.J.6
Mueller, R.F.7
Markham, A.F.8
-
14
-
-
79958820932
-
Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature
-
Abou Jamra R, Philippe O, Raas-Rothschild A, Eck SH, Graf E, Buchert R, Borck G, Ekici A, Brockschmidt FF, Nothen MM, Munnich A, Strom TM, Reis A, Colleaux L (2011) Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature. Am J Hum Genet 88(6):788-795
-
(2011)
Am J Hum Genet
, vol.88
, Issue.6
, pp. 788-795
-
-
Abou Jamra, R.1
Philippe, O.2
Raas-Rothschild, A.3
Eck, S.H.4
Graf, E.5
Buchert, R.6
Borck, G.7
Ekici, A.8
Brockschmidt, F.F.9
Nothen, M.M.10
Munnich, A.11
Strom, T.M.12
Reis, A.13
Colleaux, L.14
-
15
-
-
0142219836
-
Adaptor protein complex-4 (AP-4) is expressed in the central nervous system neurons and interacts with gluta-mate receptor delta2
-
Yap CC, Murate M, Kishigami S, Muto Y, Kishida H, Hashikawa T, Yano R (2003) Adaptor protein complex-4 (AP-4) is expressed in the central nervous system neurons and interacts with gluta-mate receptor delta2. Mol Cell Neurosci 24(2):283-295
-
(2003)
Mol Cell Neurosci
, vol.24
, Issue.2
, pp. 283-295
-
-
Yap, C.C.1
Murate, M.2
Kishigami, S.3
Muto, Y.4
Kishida, H.5
Hashikawa, T.6
Yano, R.7
-
16
-
-
40249109892
-
Accumulation of AMPA receptors in autophagosomes in neuronal axons lacking adaptor protein AP-4
-
Matsuda S, Miura E, Matsuda K, Kakegawa W, Kohda K, Wa-tanabe M, Yuzaki M (2008) Accumulation of AMPA receptors in autophagosomes in neuronal axons lacking adaptor protein AP-4. Neuron 57(5):730-745
-
(2008)
Neuron
, vol.57
, Issue.5
, pp. 730-745
-
-
Matsuda, S.1
Miura, E.2
Matsuda, K.3
Kakegawa, W.4
Kohda, K.5
Wa-Tanabe, M.6
Yuzaki, M.7
-
17
-
-
0029023325
-
Impairment of motor coordination. Purkinje cell synapse formation, and cerebellar long-term depression in GluR delta 2 mutant mice
-
Kashiwabuchi N, Ikeda K, Araki K, Hirano T, Shibuki K, Ta-kayama C, Inoue Y, Kutsuwada T, Yagi T, Kang Y et al (1995) Impairment of motor coordination, Purkinje cell synapse formation, and cerebellar long-term depression in GluR delta 2 mutant mice. Cell 81(2):245-252
-
(1995)
Cell
, vol.81
, Issue.2
, pp. 245-252
-
-
Kashiwabuchi, N.1
Ikeda, K.2
Araki, K.3
Hirano, T.4
Shibuki, K.5
Ta-Kayama, C.6
Inoue, Y.7
Kutsuwada, T.8
Yagi, T.9
Kang, Y.10
-
18
-
-
0031439985
-
Impaired parallel fiber-Purkinje cell synapse stabilization during cerebellar development of mutant mice lacking the glutamate receptor delta2 sub-unit
-
Kurihara H, Hashimoto K, Kano M, Takayama C, Sakimura K, Mishina M, Inoue Y, Watanabe M (1997) Impaired parallel fiber-[Purkinje cell synapse stabilization during cerebellar development of mutant mice lacking the glutamate receptor delta2 sub-unit. J Neurosci 17(24):9613-9623
-
(1997)
J Neurosci
, vol.17
, Issue.24
, pp. 9613-9623
-
-
Kurihara, H.1
Hashimoto, K.2
Kano, M.3
Takayama, C.4
Sakimura, K.5
Mishina, M.6
Inoue, Y.7
Watanabe, M.8
-
19
-
-
0141894133
-
Neuronal polarity and trafficking
-
Horton AC, Ehlers MD (2003) Neuronal polarity and trafficking. Neuron 40(2):277-295
-
(2003)
Neuron
, vol.40
, Issue.2
, pp. 277-295
-
-
Horton, A.C.1
Ehlers, M.D.2
-
20
-
-
0037926396
-
Disruption of the endocytic protein HIP1 results in neurological deficits and decreased AMPA receptor trafficking
-
Metzler M, Li B, Gan L, Georgiou J, Gutekunst CA, Wang Y, Torre E, Devon RS, Oh R, Legendre-Guillemin V, Rich M, Alvarez C, Gertsenstein M, McPherson PS, Nagy A, Wang YT, Roder JC, Raymond LA, Hayden MR (2003) Disruption of the endocytic protein HIP1 results in neurological deficits and decreased AMPA receptor trafficking. EMBO J 22(13):3254-3266
-
(2003)
EMBO J
, vol.22
, Issue.13
, pp. 3254-3266
-
-
Metzler, M.1
Li, B.2
Gan, L.3
Georgiou, J.4
Gutekunst, C.A.5
Wang, Y.6
Torre, E.7
Devon, R.S.8
Oh, R.9
Legendre-Guillemin, V.10
Rich, M.11
Alvarez, C.12
Gertsenstein, M.13
McPherson, P.S.14
Nagy, A.15
Wang, Y.T.16
Roder, J.C.17
Raymond, L.A.18
Hayden, M.R.19
-
21
-
-
79551651120
-
Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
-
Moreno-De-Luca A, Helmers SL, Mao H, Burns TG, Melton AM, Schmidt KR, Fernhoff PM, Ledbetter DH, Martin CL (2011) Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability. J Med Genet 48(2):141-144
-
(2011)
J Med Genet
, vol.48
, Issue.2
, pp. 141-144
-
-
Moreno-De-Luca, A.1
Helmers, S.L.2
Mao, H.3
Burns, T.G.4
Melton, A.M.5
Schmidt, K.R.6
Fernhoff, P.M.7
Ledbetter, D.H.8
Martin, C.L.9
-
22
-
-
67649587137
-
Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy
-
Verkerk AJ, Schot R, Dumee B, Schellekens K, Swagemakers S, Bertoli-Avella AM, Lequin MH, Dudink J, Govaert P, van Zwol AL, Hirst J, Wessels MW, Catsman-Berrevoets C, Verheijen FW, de Graaff E, de Coo IF, Kros JM, Willemsen R, Willems PJ, van der Spek PJ, Mancini GM (2009) Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy. Am J Hum Genet 85(1):40-52
-
(2009)
Am J Hum Genet
, vol.85
, Issue.1
, pp. 40-52
-
-
Verkerk, A.J.1
Schot, R.2
Dumee, B.3
Schellekens, K.4
Swagemakers, S.5
Bertoli-Avella, A.M.6
Lequin, M.H.7
Dudink, J.8
Govaert, P.9
Van Zwol, A.L.10
Hirst, J.11
Wessels, M.W.12
Catsman-Berrevoets, C.13
Verheijen, F.W.14
De Graaff, E.15
De Coo, I.F.16
Kros, J.M.17
Willemsen, R.18
Willems, P.J.19
Van Der Spek, P.J.20
Mancini, G.M.21
more..
-
23
-
-
80053906761
-
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
-
Najmabadi H, Hu H, Garshasbi M, Zemojtel T, Abedini SS, Chen W, Hosseini M, Behjati F, Haas S, Jamali P, Zecha A, Mohseni M, Puttmann L, Vahid LN, Jensen C, Moheb LA, Bienek M, Larti F, Mueller I, Weissmann R, Darvish H, Wrogemann K, Hadavi V, Lipkowitz B, Esmaeeli-Nieh S, Wieczorek D, Kariminejad R, Firouzabadi SG, Cohen M, Fattahi Z, Rost I, Mojahedi F, Hertzberg C, Dehghan A, Rajab A, Banavandi MJ, Hoffer J, Falah M, Musante L, Kalscheuer V, Ullmann R, Kuss AW, Tzschach A, Kahrizi K, Ropers HH (2011) Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature 478(7367):57-63
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 57-63
-
-
Najmabadi, H.1
Hu, H.2
Garshasbi, M.3
Zemojtel, T.4
Abedini, S.S.5
Chen, W.6
Hosseini, M.7
Behjati, F.8
Haas, S.9
Jamali, P.10
Zecha, A.11
Mohseni, M.12
Puttmann, L.13
Vahid, L.N.14
Jensen, C.15
Moheb, L.A.16
Bienek, M.17
Larti, F.18
Mueller, I.19
Weissmann, R.20
Darvish, H.21
Wrogemann, K.22
Hadavi, V.23
Lipkowitz, B.24
Esmaeeli-Nieh, S.25
Wieczorek, D.26
Kariminejad, R.27
Firouzabadi, S.G.28
Cohen, M.29
Fattahi, Z.30
Rost, I.31
Mojahedi, F.32
Hertzberg, C.33
Dehghan, A.34
Rajab, A.35
Banavandi, M.J.36
Hoffer, J.37
Falah, M.38
Musante, L.39
Kalscheuer, V.40
Ullmann, R.41
Kuss, A.W.42
Tzschach, A.43
Kahrizi, K.44
Ropers, H.H.45
more..
-
24
-
-
84861318140
-
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)
-
Bauer P, Leshinsky-Silver E, Blumkin L, Schlipf N, Schroder C, Schicks J, Lev D, Riess O, Lerman-Sagie T, Schols L (2012) Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47). Neurogenetics 13(1):73-76
-
(2012)
Neurogenetics
, vol.13
, Issue.1
, pp. 73-76
-
-
Bauer, P.1
Leshinsky-Silver, E.2
Blumkin, L.3
Schlipf, N.4
Schroder, C.5
Schicks, J.6
Lev, D.7
Riess, O.8
Lerman-Sagie, T.9
Schols, L.10
-
25
-
-
0034537673
-
Surveillance of cerebral palsy in Europe: A collaboration of cerebral palsy surveys and registers. Surveillance of Cerebral Palsy in Europe (SCPE)
-
Cans C (2000) Surveillance of cerebral palsy in Europe: a collaboration of cerebral palsy surveys and registers. Surveillance of Cerebral Palsy in Europe (SCPE). Dev Med Child Neurol 42:816-824
-
(2000)
Dev Med Child Neurol
, vol.42
, pp. 816-824
-
-
Cans, C.1
-
26
-
-
67749137294
-
Erythro-poietin improved neurologic outcomes in newborns with hyp-oxic-ischemic encephalopathy
-
Zhu C, Kang W, Xu F, Cheng X, Zhang Z, Jia L, Ji L, Guo X, Xiong H, Simbruner G, Blomgren K, Wang X (2009) Erythro-poietin improved neurologic outcomes in newborns with hyp-oxic-ischemic encephalopathy. Pediatrics 124(2):e218-e226
-
(2009)
Pediatrics
, vol.124
, Issue.2
-
-
Zhu, C.1
Kang, W.2
Xu, F.3
Cheng, X.4
Zhang, Z.5
Jia, L.6
Ji, L.7
Guo, X.8
Xiong, H.9
Simbruner, G.10
Blomgren, K.11
Wang, X.12
-
27
-
-
70350686646
-
Neonatal brain imaging and the identification of metabolic acidemia and hypoxic-ischemic encephalopathy
-
Ruis KA, Lehmann CU, Northington FJ, Lin DD, Graham EM (2009) Neonatal brain imaging and the identification of metabolic acidemia and hypoxic-ischemic encephalopathy. J Matern Fetal Neonatal Med 22(10):823-828
-
(2009)
J Matern Fetal Neonatal Med
, vol.22
, Issue.10
, pp. 823-828
-
-
Ruis, K.A.1
Lehmann, C.U.2
Northington, F.J.3
Lin, D.D.4
Graham, E.M.5
-
28
-
-
34547145165
-
G*power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences
-
Faul F, Erdfelder E, Lang AG, Buchner A (2007) G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods 39(2):175-191
-
(2007)
Behav Res Methods
, vol.39
, Issue.2
, pp. 175-191
-
-
Faul, F.1
Erdfelder, E.2
Lang, A.G.3
Buchner, A.4
-
30
-
-
67651121993
-
The genomic basis of cerebral palsy: A HuGE systematic literature review
-
O'Callaghan ME, MacLennan AH, Haan EA, Dekker G (2009) The genomic basis of cerebral palsy: a HuGE systematic literature review. Hum Genet 126:149-172
-
(2009)
Hum Genet
, vol.126
, pp. 149-172
-
-
O'Callaghan, M.E.1
Maclennan, A.H.2
Haan, E.A.3
Dekker, G.4
-
31
-
-
53849097342
-
Asphyxia-related risk factors and their timing in spastic cerebral palsy
-
Nielsen LF, Schendel D, Grove J, Hvidtjorn D, Jacobsson B, Josiassen T, Vestergaard M, Uldall P, Thorsen P (2008) Asphyxia-related risk factors and their timing in spastic cerebral palsy. BJOG 115(12):1518-1528
-
(2008)
BJOG
, vol.115
, Issue.12
, pp. 1518-1528
-
-
Nielsen, L.F.1
Schendel, D.2
Grove, J.3
Hvidtjorn, D.4
Jacobsson, B.5
Josiassen, T.6
Vestergaard, M.7
Uldall, P.8
Thorsen, P.9
-
32
-
-
0017744466
-
Recurrence risks in families of children with symmetrical spasticity
-
Bundey S, Griffiths MI (1977) Recurrence Risks in Families of Children with Symmetrical Spasticity. Dev Med Child Neurol 19(2):179-191
-
(1977)
Dev Med Child Neurol
, vol.19
, Issue.2
, pp. 179-191
-
-
Bundey, S.1
Griffiths, M.I.2
-
33
-
-
0027373170
-
Excitatory amino-acids in the cerebrospinal-fluid of asphyxiated infants-relationship to hypoxic-ischemic encephalopathy
-
Hagberg H, Thornberg E, Blennow M, Kjellmer I, Lagercrantz H, Thiringer K, Hamberger A, Sandberg M (1993) Excitatory amino-acids in the cerebrospinal-fluid of asphyxiated infants-relationship to hypoxic-ischemic encephalopathy. Acta Paediatr 82(11):925-929
-
(1993)
Acta Paediatr
, vol.82
, Issue.11
, pp. 925-929
-
-
Hagberg, H.1
Thornberg, E.2
Blennow, M.3
Kjellmer, I.4
Lagercrantz, H.5
Thiringer, K.6
Hamberger, A.7
Sandberg, M.8
-
34
-
-
0034003123
-
Increased detectability of alpha brain gluta-mate/glutamine in neonatal hypoxic-ischemic encephalopathy
-
Pu YL, Li QF, Zeng CM, Gao J, Qi J, Luo DX, Mahankali S, Fox PT, Gao JH (2000) Increased detectability of alpha brain gluta-mate/glutamine in neonatal hypoxic-ischemic encephalopathy. Am J Neuroradiol 21(1):203-212
-
(2000)
Am J Neuroradiol
, vol.21
, Issue.1
, pp. 203-212
-
-
Pu, Y.L.1
Li, Q.F.2
Zeng, C.M.3
Gao, J.4
Qi, J.5
Luo, D.X.6
Mahankali, S.7
Fox, P.T.8
Gao, J.H.9
-
35
-
-
23844536093
-
Excitotoxicity in perinatal brain injury
-
Johnston MV (2005) Excitotoxicity in perinatal brain injury. Brain Pathol 15(3):234-240
-
(2005)
Brain Pathol
, vol.15
, Issue.3
, pp. 234-240
-
-
Johnston, M.V.1
-
36
-
-
34548331835
-
Delayed IGF-1 administration rescues oligodendrocyte progenitors from glutamate-induced cell death and hypoxic-ischemic brain damage
-
Wood TL, Loladze V, Altieri S, Gangoli N, Levison SW, Brywe KG, Mallard C, Hagberg H (2007) Delayed IGF-1 administration rescues oligodendrocyte progenitors from glutamate-induced cell death and hypoxic-ischemic brain damage. Dev Neurosci 29(4-5):302-310
-
(2007)
Dev Neurosci
, vol.29
, Issue.4-5
, pp. 302-310
-
-
Wood, T.L.1
Loladze, V.2
Altieri, S.3
Gangoli, N.4
Levison, S.W.5
Brywe, K.G.6
Mallard, C.7
Hagberg, H.8
-
37
-
-
65549107439
-
Neuroprotection by the NR3A subunit of the NMDA receptor
-
Nakanishi N, Tu S, Shin Y, Cui J, Kurokawa T, Zhang D, Chen HS, Tong G, Lipton SA (2009) Neuroprotection by the NR3A subunit of the NMDA receptor. J Neurosci 29(16):5260-5265
-
(2009)
J Neurosci
, vol.29
, Issue.16
, pp. 5260-5265
-
-
Nakanishi, N.1
Tu, S.2
Shin, Y.3
Cui, J.4
Kurokawa, T.5
Zhang, D.6
Chen, H.S.7
Tong, G.8
Lipton, S.A.9
-
38
-
-
84862753773
-
Increased concentrations of both NMDA receptor co-agonists D-serine and glycine in global ischemia: A potential novel treatment target for perinatal asphyxia
-
Fuchs SA, Peeters-Scholte CMPCD, de Barse MMJ, Roeleveld MW, Klomp LWJ, Berger R, de Koning TJ (2012) Increased concentrations of both NMDA receptor co-agonists D-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxia. Amino Acids 43(1):355-363
-
(2012)
Amino Acids
, vol.43
, Issue.1
, pp. 355-363
-
-
Fuchs, S.A.1
Cmpcd, P.2
De Barse, M.M.J.3
Roeleveld, M.W.4
Klomp, L.W.J.5
Berger, R.6
De Koning, T.J.7
-
39
-
-
23844536093
-
Excitotoxicity in perinatal brain injury
-
Johnston MV (2005) Excitotoxicity in perinatal brain injury. Brain Pathol 15(3):234-240
-
(2005)
Brain Pathol
, vol.15
, Issue.3
, pp. 234-240
-
-
Johnston, M.V.1
-
41
-
-
5044235541
-
Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins
-
Fernandez-Escamilla AM, Rousseau F, Schymkowitz J, Serrano L (2004) Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins. Nat Bio-technol 22(10):1302-1306
-
(2004)
Nat Bio-technol
, vol.22
, Issue.10
, pp. 1302-1306
-
-
Fernandez-Escamilla, A.M.1
Rousseau, F.2
Schymkowitz, J.3
Serrano, L.4
-
42
-
-
4143134235
-
The future of association studies: Gene-based analysis and replication
-
Neale BM, Sham PC (2004) The future of association studies: gene-based analysis and replication. Am J Hum Genet 75(3):353-362
-
(2004)
Am J Hum Genet
, vol.75
, Issue.3
, pp. 353-362
-
-
Neale, B.M.1
Sham, P.C.2
|