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Gardiner, Alice R.
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1

The need for biochemical testing in beta‐enolase deficiency..:

Wigley, Ralph ; Scalco, Renata S. ; Gardiner, Alice R....
JIMD Reports.  50 (2019)  1 - p. 40-43 , 2019
Link: https://doi.org/10.1002/..
 
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2

GYG1 causing progressive limb girdle myopathy with onset du..:

Desikan, Mahalekshmi ; Scalco, Renata Siciliani ; Manole, Andreea...
Neuromuscular Disorders.  28 (2018)  4 - p. 346-349 , 2018
Link: https://doi.org/10.1016/..
 
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3

CAV3 mutations causing exercise intolerance, myalgia and rh..:

Scalco, Renata Siciliani ; Gardiner, Alice R. ; Pitceathly, Robert D.S....
Neuromuscular Disorders.  26 (2016)  8 - p. 504-510 , 2016
Link: https://doi.org/10.1016/..
 
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4

The clinical and genetic heterogeneity of paroxysmal dyskin..:

Gardiner, Alice R. ; Jaffer, Fatima ; Dale, Russell C....
Brain.  138 (2015)  12 - p. 3567-3580 , 2015
Link: https://doi.org/10.1093/..
 
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5

Rhabdomyolysis: a genetic perspective:

Scalco, Renata Siciliani ; Gardiner, Alice R ; Pitceathly, Robert DS...
Orphanet Journal of Rare Diseases.  10 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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6

Clinical features of childhood‐onset paroxysmal kinesigenic..:

Silveira‐Moriyama, Laura ; Gardiner, Alice R ; Meyer, Esther...
Developmental Medicine & Child Neurology.  55 (2013)  4 - p. 327-334 , 2013
Link: https://doi.org/10.1111/..
 
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7

PRRT2gene mutations: From paroxysmal dyskinesia to episodic..:

Gardiner, Alice R. ; Bhatia, Kailash P. ; Stamelou, Maria...
Neurology.  79 (2012)  21 - p. 2115-2121 , 2012
Link: https://doi.org/10.1212/..
 
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8

The need for biochemical testing in beta‐enolase deficiency..:

Wigley, Ralph ; Scalco, Renata S ; Gardiner, Alice R...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851005/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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9

CAV3 mutations causing exercise intolerance, myalgia and rh..:

Scalco, Renata Siciliani ; Gardiner, Alice R ; Pitceathly, Robert D.S...
Scalco , R S , Gardiner , A R , Pitceathly , R D S , Hilton-Jones , D , Schapira , A H , Turner , C , Parton , M , Desikan , M , Barresi , R , Marsh , J , Manzur , A Y , Childs , A-M , Feng , L , Murphy , E , Lamont , P J , Ravenscroft , G , Wallefeld , W , Davis , M R , Laing , N G , Holton , J L , Fialho , D , Bushby , K , Hanna , M G , Phadke , R , Jungbluth , H , Houlden , H & Quinlivan , R 2016 , ' CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: expanding the phenotypic spectrum of caveolinopathies ' , Neuromuscular Disorders , vol. 26 , no. 8 , pp. 504-510 . https://doi.org/10.1016/j.nmd.2016.05.006.  , 2016
Link: https://kclpure.kcl.ac.u..
 
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10

CAV3 mutations causing exercise intolerance, myalgia and rh..:

Scalco, Renata Siciliani ; Gardiner, Alice R ; Pitceathly, Robert D.S...
Scalco , R S , Gardiner , A R , Pitceathly , R D S , Hilton-Jones , D , Schapira , A H , Turner , C , Parton , M , Desikan , M , Barresi , R , Marsh , J , Manzur , A Y , Childs , A-M , Feng , L , Murphy , E , Lamont , P J , Ravenscroft , G , Wallefeld , W , Davis , M R , Laing , N G , Holton , J L , Fialho , D , Bushby , K , Hanna , M G , Phadke , R , Jungbluth , H , Houlden , H & Quinlivan , R 2016 , ' CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: expanding the phenotypic spectrum of caveolinopathies ' , Neuromuscular Disorders , vol. 26 , no. 8 , pp. 504-510 . https://doi.org/10.1016/j.nmd.2016.05.006.  , 2016
Link: https://kclpure.kcl.ac.u..
 
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11

Rhabdomyolysis:A genetic perspective:

Scalco, Renata Siciliani ; Gardiner, Alice R ; Pitceathly, Robert Ds...
Scalco , R S , Gardiner , A R , Pitceathly , R D , Zanoteli , E , Becker , J , Holton , J L , Houlden , H , Jungbluth , H & Quinlivan , R 2015 , ' Rhabdomyolysis : A genetic perspective ' , Orphanet Journal of Rare Diseases , vol. 10 , no. 1 , 51 . https://doi.org/10.1186/s13023-015-0264-3.  , 2015
Link: https://kclpure.kcl.ac.u..
 
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12

Rhabdomyolysis:A genetic perspective:

Scalco, Renata Siciliani ; Gardiner, Alice R ; Pitceathly, Robert Ds...
Scalco , R S , Gardiner , A R , Pitceathly , R D , Zanoteli , E , Becker , J , Holton , J L , Houlden , H , Jungbluth , H & Quinlivan , R 2015 , ' Rhabdomyolysis : A genetic perspective ' , Orphanet Journal of Rare Diseases , vol. 10 , no. 1 , 51 . https://doi.org/10.1186/s13023-015-0264-3.  , 2015
Link: https://kclpure.kcl.ac.u..
 
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13

Clinical features of childhood-onset paroxysmal kinesigenic..:

Silveira-Moriyama, Laura ; Gardiner, Alice R ; Meyer, Esther...
Silveira-Moriyama , L , Gardiner , A R , Meyer , E , King , M D , Smith , M , Rakshi , K , Parker , A , Mallick , A A , Brown , R , Vassallo , G , Jardine , P E , Guerreiro , M M , Lees , A J , Houlden , H & Kurian , M A 2013 , ' Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations ' , Developmental Medicine and Child Neurology , vol. 55 , no. 4 , pp. 327-334 . https://doi.org/10.1111/dmcn.12056.  , 2013
Link: https://hdl.handle.net/1..
 
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14

PRRT2 gene mutations: From paroxysmal dyskinesia to episodi..:

Gardiner, Alice R ; Bhatia, Kailash P ; Stamelou, Maria...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511930.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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15

Autologous granulosa cell coculture demonstrates zygote sup..:

Seifer, David B. ; Freeman, Melanie R. ; Gardiner, Alice C....
Fertility and Sterility.  66 (1996)  3 - p. 425-429 , 1996
Link: https://doi.org/10.1016/..
 
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