|
🐜
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The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study
9 auth.
J. Phukan,
M. Elamin,
P. Bede,
N. Jordan,
L. Gallagher,
S. Byrne,
...
C. Lynch,
N. Pender,
O. Hardiman
|
9 |
2011 |
9
🐜
|
|
🐜
|
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
20 auth.
S. Byrne,
M. Elamin,
P. Bede,
A. Shatunov,
C. Walsh,
B. Corr,
M. Heverin,
N. Jordan,
K. Kenna,
C. Lynch,
...
R. Mclaughlin,
P. Iyer,
Caoimhe O'Brien,
J. Phukan,
Brona Wynne,
A. Bokde,
D. Bradley,
N. Pender,
A. Al-Chalabi,
Orla Hardiman
|
8 |
2012 |
8
🐜
|
|
🐜
|
Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis
8 auth.
S. Byrne,
C. Walsh,
C. Lynch,
P. Bede,
M. Elamin,
K. Kenna,
...
R. Mclaughlin,
O. Hardiman
|
8 |
2010 |
8
🐜
|
|
🐜
|
Long term trends in prevalence of neural tube defects in Europe: population based study
30 auth.
B. Khoshnood,
M. Loane,
H. D. de Walle,
L. Arriola,
M. Addor,
I. Barišić,
J. Béres,
F. Bianchi,
C. Dias,
E. Draper,
E. Garne,
M. Gatt,
M. Haeusler,
K. Klungsøyr,
A. Latos-Bieleńska,
...
C. Lynch,
B. McDonnell,
V. Nelen,
A. Neville,
M. O’Mahony,
A. Queisser‐Luft,
J. Rankin,
A. Rissmann,
A. Ritvanen,
C. Rounding,
A. Sipek,
D. Tucker,
C. Verellen‐Dumoulin,
D. Wellesley,
H. Dolk
|
7 |
2015 |
7
🐜
|
|
🐜
|
Cognitive changes predict functional decline in ALS
11 auth.
M. Elamin,
P. Bede,
S. Byrne,
N. Jordan,
L. Gallagher,
Brona Wynne,
...
Caoimhe O'Brien,
J. Phukan,
C. Lynch,
N. Pender,
O. Hardiman
|
7 |
2013 |
7
🐜
|
|
🐜
|
Proposed criteria for familial amyotrophic lateral sclerosis
7 auth.
S. Byrne,
P. Bede,
M. Elamin,
K. Kenna,
C. Lynch,
R. Mclaughlin,
...
O. Hardiman
|
7 |
2011 |
7
🐜
|
|
🐜
|
Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality
12 auth.
P. Bede,
A. Bokde,
M. Elamin,
S. Byrne,
R. Mclaughlin,
N. Jordan,
...
H. Hampel,
L. Gallagher,
C. Lynch,
A. Fagan,
N. Pender,
O. Hardiman
|
7 |
2012 |
7
🐜
|
|
🐜
|
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: A population‐based case–control cohort study of familial and sporadic amyotrophic lateral sclerosis
10 auth.
S. Byrne,
M. Heverin,
M. Elamin,
P. Bede,
C. Lynch,
K. Kenna,
...
R. MacLaughlin,
C. Walsh,
A. Chalabi,
O. Hardiman
|
6 |
2013 |
6
🐜
|
|
🐜
|
Trends in congenital anomalies in Europe from 1980 to 2012
30 auth.
J. Morris,
A. Springett,
R. Greenlees,
M. Loane,
M. Addor,
L. Arriola,
I. Barišić,
J. Bergman,
M. Csáky‐Szunyogh,
C. Dias,
E. Draper,
E. Garne,
M. Gatt,
B. Khoshnood,
K. Klungsøyr,
...
C. Lynch,
R. McDonnell,
V. Nelen,
A. Neville,
M. O’Mahony,
A. Pierini,
A. Queisser‐Luft,
H. Randrianaivo,
J. Rankin,
A. Rissmann,
J. Kurinczuk,
D. Tucker,
C. Verellen‐Dumoulin,
D. Wellesley,
H. Dolk
|
6 |
2018 |
6
🐜
|
|
🐜
|
Congenital anomalies associated with trisomy 18 or trisomy 13: A registry‐based study in 16 european countries, 2000–2011
29 auth.
A. Springett,
D. Wellesley,
R. Greenlees,
M. Loane,
M. Addor,
L. Arriola,
J. Bergman,
C. Cavero-Carbonell,
M. Csáky‐Szunyogh,
E. Draper,
E. Garne,
M. Gatt,
M. Haeusler,
B. Khoshnood,
K. Klungsøyr,
...
C. Lynch,
Carlos Matias Dias,
R. McDonnell,
V. Nelen,
M. O’Mahony,
A. Pierini,
A. Queisser‐Luft,
J. Rankin,
A. Rissmann,
C. Rounding,
S. Stoianova,
David Tuckerz,
Natalya Zymak-Zakutnia,
J. Morris
|
6 |
2015 |
6
🐜
|
|
🐜
|
Prevalence of microcephaly in Europe: population based study
30 auth.
J. Morris,
J. Rankin,
E. Garne,
M. Loane,
R. Greenlees,
M. Addor,
L. Arriola,
I. Barišić,
J. Bergman,
M. Csáky‐Szunyogh,
C. Dias,
E. Draper,
M. Gatt,
B. Khoshnood,
K. Klungsøyr,
...
J. Kurinczuk,
C. Lynch,
R. McDonnell,
V. Nelen,
A. Neville,
M. O’Mahony,
A. Pierini,
H. Randrianaivo,
A. Rissmann,
D. Tucker,
C. Verellen‐Dumoulin,
H. D. de Walle,
D. Wellesley,
Awi Wiesel,
H. Dolk
|
6 |
2016 |
6
🐜
|
