共 30 条
[21]
Filamins: promiscuous organizers of the cytoskeleton
[J].
Popowicz, Grzegorz M.
;
Schleicher, Michael
;
Noegel, Angelika A.
;
Holak, Tad A.
.
TRENDS IN BIOCHEMICAL SCIENCES,
2006, 31 (07)
:411-419

Popowicz, Grzegorz M.
论文数: 0 引用数: 0
h-index: 0
机构: Max Planck Inst Biochem, D-82152 Martinsried, Germany

Schleicher, Michael
论文数: 0 引用数: 0
h-index: 0
机构: Max Planck Inst Biochem, D-82152 Martinsried, Germany

Noegel, Angelika A.
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Biochem, D-82152 Martinsried, Germany Max Planck Inst Biochem, D-82152 Martinsried, Germany

Holak, Tad A.
论文数: 0 引用数: 0
h-index: 0
机构: Max Planck Inst Biochem, D-82152 Martinsried, Germany
[22]
Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans
[J].
Robertson, SP
;
Twigg, SRF
;
Sutherland-Smith, AJ
;
Biancalana, V
;
Gorlin, RJ
;
Horn, D
;
Kenwrick, SJ
;
Kim, CA
;
Morava, E
;
Newbury-Ecob, R
;
Orstavik, KH
;
Quarrell, OWJ
;
Schwartz, CE
;
Shears, DJ
;
Suri, M
;
Kendrick-Jones, J
;
Wilkie, AOM
.
NATURE GENETICS,
2003, 33 (04)
:487-491

Robertson, SP
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Twigg, SRF
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Sutherland-Smith, AJ
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Biancalana, V
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Gorlin, RJ
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Horn, D
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Kenwrick, SJ
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Kim, CA
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Morava, E
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Newbury-Ecob, R
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Orstavik, KH
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Quarrell, OWJ
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Schwartz, CE
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Shears, DJ
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Suri, M
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Kendrick-Jones, J
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England

Wilkie, AOM
论文数: 0 引用数: 0
h-index: 0
机构: City Hosp, Clin Genet Serv, Nottingham NG5 1PB, England
[23]
Filamin A: phenotypic diversity
[J].
Robertson, SP
.
CURRENT OPINION IN GENETICS & DEVELOPMENT,
2005, 15 (03)
:301-307

Robertson, SP
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Otago, Dunedin Sch Med, Dept Paediat & Child Hlth, Dunedin, New Zealand Univ Otago, Dunedin Sch Med, Dept Paediat & Child Hlth, Dunedin, New Zealand
[24]
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome
[J].
Sheen, VL
;
Jansen, A
;
Chen, MH
;
Parrini, E
;
Morgan, T
;
Ravenscroft, R
;
Ganesh, V
;
Underwood, T
;
Wiley, J
;
Leventer, R
;
Vaid, RR
;
Ruiz, DE
;
Hutchins, GM
;
Menasha, J
;
Willner, J
;
Geng, Y
;
Gripp, KW
;
Nicholson, L
;
Berry-Kravis, E
;
Bodell, A
;
Apse, K
;
Hill, RS
;
Dubeau, F
;
Andermann, F
;
Barkovich, J
;
Andermann, E
;
Shugart, YY
;
Thomas, P
;
Viri, M
;
Veggiotti, P
;
Robertson, S
;
Guerrini, R
;
Walsh, CA
.
NEUROLOGY,
2005, 64 (02)
:254-262

Sheen, VL
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Jansen, A
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Chen, MH
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Parrini, E
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Morgan, T
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Ravenscroft, R
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Ganesh, V
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Underwood, T
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Wiley, J
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Leventer, R
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Vaid, RR
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Ruiz, DE
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Hutchins, GM
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Menasha, J
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Willner, J
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Geng, Y
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Gripp, KW
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Nicholson, L
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Berry-Kravis, E
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Bodell, A
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Apse, K
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Hill, RS
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Dubeau, F
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Andermann, F
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Barkovich, J
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Andermann, E
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Shugart, YY
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Thomas, P
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Viri, M
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Veggiotti, P
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Robertson, S
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Guerrini, R
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA

Walsh, CA
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA
[25]
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females
[J].
Sheen, VL
;
Dixon, PH
;
Fox, JW
;
Hong, SE
;
Kinton, L
;
Sisodiya, SM
;
Duncan, JS
;
Dubeau, F
;
Scheffer, IE
;
Schachter, SC
;
Wilner, A
;
Henchy, R
;
Crino, P
;
Kamuro, K
;
DiMario, F
;
Berg, M
;
Kuzniecky, R
;
Cole, AJ
;
Bromfield, E
;
Biber, M
;
Schomer, D
;
Wheless, J
;
Silver, K
;
Mochida, GH
;
Berkovic, SF
;
Andermann, F
;
Andermann, E
;
Dobyns, WB
;
Wood, NW
;
Walsh, CA
.
HUMAN MOLECULAR GENETICS,
2001, 10 (17)
:1775-1783

Sheen, VL
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Dixon, PH
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Fox, JW
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Hong, SE
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Kinton, L
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Sisodiya, SM
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Duncan, JS
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Dubeau, F
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Scheffer, IE
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Schachter, SC
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Wilner, A
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Henchy, R
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Crino, P
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Kamuro, K
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

DiMario, F
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Berg, M
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Kuzniecky, R
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Cole, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Bromfield, E
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Biber, M
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Schomer, D
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Wheless, J
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Silver, K
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Mochida, GH
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Berkovic, SF
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Andermann, F
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Andermann, E
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Dobyns, WB
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Wood, NW
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA

Walsh, CA
论文数: 0 引用数: 0
h-index: 0
机构: Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02115 USA
[26]
Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact
[J].
Sheen, VL
;
Feng, YY
;
Graham, D
;
Takafuta, T
;
Shapiro, SS
;
Walsh, CA
.
HUMAN MOLECULAR GENETICS,
2002, 11 (23)
:2845-2854

Sheen, VL
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA

Feng, YY
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA

Graham, D
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA

Takafuta, T
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA

Shapiro, SS
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA

Walsh, CA
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Inst Med, Div Neurogenet, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[27]
Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations
[J].
Sole, G.
;
Coupry, I.
;
Rooryck, C.
;
Guerineau, E.
;
Martins, F.
;
Deves, S.
;
Hubert, C.
;
Souakri, N.
;
Boute, O.
;
Marchal, C.
;
Faivre, L.
;
Landre, E.
;
Debruxelles, S.
;
Dieux-Coeslier, A.
;
Boulay, C.
;
Chassagnon, S.
;
Michel, V.
;
Routon, M-C
;
Toutain, A.
;
Philip, N.
;
Lacombe, D.
;
Villard, L.
;
Arveiler, B.
;
Goizet, C.
.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
2009, 80 (12)
:1394-1398

Sole, G.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
Hop Pellegrin, CHU Bordeaux, Fed Neurosci Clin, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Coupry, I.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Rooryck, C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
Hop Pellegrin Enfants, Serv Genet Med, CHU Bordeaux, Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Guerineau, E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Martins, F.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Deves, S.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Pellegrin Enfants, Serv Genet Med, CHU Bordeaux, Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Hubert, C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Souakri, N.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Boute, O.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Jeanne de Flandre, Serv Genet Clin, CHU Lille, Lille, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Marchal, C.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Pellegrin, CHU Bordeaux, Fed Neurosci Clin, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Faivre, L.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Enfants, Ctr Genet, CHU Dijon, Dijon, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Landre, E.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop St Anne, Ctr Neurochirurg, CHU Cochin Port Royal, F-75674 Paris, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Debruxelles, S.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Pellegrin, CHU Bordeaux, Fed Neurosci Clin, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Dieux-Coeslier, A.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Jeanne de Flandre, Serv Genet Clin, CHU Lille, Lille, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Boulay, C.
论文数: 0 引用数: 0
h-index: 0
机构:
CH Mulhouse, Serv Neurol & Explorat Fonct Syst Nerveux & Neuro, Mulhouse, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Chassagnon, S.
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Strasbourg, Dept Neurol, F-67000 Strasbourg, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Michel, V.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Pellegrin, CHU Bordeaux, Fed Neurosci Clin, F-33076 Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Routon, M-C
论文数: 0 引用数: 0
h-index: 0
机构:
CHG Orsay, Serv Pediat & Neonatol, Orsay, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Toutain, A.
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Bretonneau, CHU Tours, Serv Genet Med, Tours, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Philip, N.
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h-index: 0
机构:
Hop Enfants La Timone, Dept Med Genet, APHM Marseille, Marseille, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Lacombe, D.
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h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
Hop Pellegrin Enfants, Serv Genet Med, CHU Bordeaux, Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Villard, L.
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机构: Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Arveiler, B.
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h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
Hop Pellegrin Enfants, Serv Genet Med, CHU Bordeaux, Bordeaux, France
Fac Med La Timone, INSERM, U910, Marseille, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France

Goizet, C.
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h-index: 0
机构:
Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
Hop Pellegrin, CHU Bordeaux, Fed Neurosci Clin, F-33076 Bordeaux, France
Hop Pellegrin Enfants, Serv Genet Med, CHU Bordeaux, Bordeaux, France Univ Victor Segalen Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France
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The clinical spectrum of nodular heterotopias in children: Report of 31 patients
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Srour, Myriam
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h-index: 0
机构:
Univ Montreal, Ctr Rech CHUM, Montreal, PQ, Canada Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Rioux, Marie-France
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h-index: 0
机构:
Univ Sherbrooke, CHU Sherbrooke, Sherbrooke, PQ J1K 2R1, Canada Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Varga, Caroline
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h-index: 0
机构:
Univ Sherbrooke, CHU Sherbrooke, Sherbrooke, PQ J1K 2R1, Canada Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Lortie, Anne
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h-index: 0
机构: Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Major, Philippe
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h-index: 0
机构: Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Robitaille, Yves
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h-index: 0
机构: Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Decarie, Jean-Claude
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h-index: 0
机构: Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Michaud, Jacques
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机构: Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada

Carmant, Lionel
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Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada Univ Montreal, Epilepsy Clin, Ctr Hosp Univ St Justine, Montreal, PQ H3T 1C5, Canada
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Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene
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Sun, Yu
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Sun, Yu
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机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Almomani, Rowida
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h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Aten, Emmelien
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h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Celli, Jacopo
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h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

van der Heijden, Jaap
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h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Venselaar, Hanka
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h-index: 0
机构:
UMC Nijmegen, Nijmegen Ctr Mol Life Sci, NL-6525 GA Nijmegen, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Robertson, Stephen P.
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h-index: 0
机构:
Univ Otago, Dept Paediat & Child Hlth, Dunedin Sch Med, Dunedin 9054, New Zealand Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Baroncini, Anna
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h-index: 0
机构:
ASL Dept Maternal & Child Hlth, Unit Med Genet, I-40026 Imola, Italy Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Franco, Brunella
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Naples Federico II, Dept Pediat, I-80131 Naples, Italy
Telethon Inst Genet & Med, I-80131 Naples, Italy Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Basel-Vanagaite, Lina
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h-index: 0
机构:
Tel Aviv Univ, Schneider Childrens Med Ctr Israel, IL-49100 Petah Tiqwa, Israel
Tel Aviv Univ, Raphael Recanati Genet Inst, Rabin Med Ctr, Petah Tikva & Sackler Fac Med, IL-49100 Petah Tiqwa, Israel Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Horii, Emiko
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h-index: 0
机构:
Nagoya 1st Red Cross Hosp, Nagoya, Aichi, Japan
Yokkaichi Municipal Hosp, Yokaichi 4538511, Japan Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Drut, Ricardo
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Ninos La Plata, Serv Pathol, RA-1900 La Plata, Argentina Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Ariyurek, Yavuz
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands
Leiden Univ, Med Ctr, Leiden Genome Technol Ctr, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

den Dunnen, Johan T.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands
Leiden Univ, Med Ctr, Leiden Genome Technol Ctr, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands

Breuning, Martijn H.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands Leiden Univ, Med Ctr, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands
[30]
A dual phenotype of periventricular nodular heterotopia and frontometaphyseal dysplasia in one patient caused by a single FLNA mutation leading to two functionally different aberrant transcripts
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Zenker, M
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Rauch, A
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Winterpacht, A
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Tagariello, A
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Kraus, C
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Rupprecht, T
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Reis, A
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AMERICAN JOURNAL OF HUMAN GENETICS,
2004, 74 (04)
:731-737

Zenker, M
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h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Rauch, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Winterpacht, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Tagariello, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Kraus, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Rupprecht, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Sticht, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

Reis, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany