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Results of search for 'au:"Ptácek, L"', page 1 of 5
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Authors
Agnew, W S
Alderson, K
Ashizawa, T
Barchi, R L
Barohn, R J
Bendahhou, S
Cummins, T R
Dalakas, M C
Digre, K B
Einum, D D
Fu, Y H
Fu, Y-H
George, A L
Griggs, R C
Jones, C R
Leppert, M
Mendell, J R
Ptacek, L J
Ptácek, L J
Tawil, R
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Adolescent
Adult
Amino Acid Sequence
Animals
Child
Chromosome Mapping
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Genetic Linkage
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Lod Score
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Middle Aged
Molecular Sequence Data
Mutation
Paralyses, Familial Periodic
Pedigree
Phenotype
Sodium Channels
genetics
metabolism
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English
Your search returned 89 results.
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1.
Ion channel shake-down.
[electronic resource]
by
Ptácek, L
Producer:
19950309
In:
Nature genetics
vol. 8
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2.
The familial periodic paralyses and nondystrophic myotonias.
[electronic resource]
by
Ptácek, L
Producer:
19980818
In:
The American journal of medicine
vol. 105
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3.
The place of migraine as a channelopathy.
[electronic resource]
by
Ptácek, L J
Producer:
19980917
In:
Current opinion in neurology
vol. 11
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4.
Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system.
[electronic resource]
by
Ptácek, L J
Producer:
19970807
In:
Neuromuscular disorders : NMD
vol. 7
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5.
Ion channel diseases: episodic disorders of the nervous system.
[electronic resource]
by
Ptácek, L J
Producer:
20000330
In:
Seminars in neurology
vol. 19
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6.
Autosomal dominant spinocerebellar atrophy with retinal degeneration.
[electronic resource]
by
Ptácek, L J
Producer:
19950824
In:
Clinical neuroscience (New York, N.Y.)
vol. 3
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7.
Ligand-gated ion channelopathies: mutations in different genes causing one disease.
[electronic resource]
by
Ptácek, L J
Producer:
20010104
In:
Neurology
vol. 55
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8.
Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system.
[electronic resource]
by
Ptácek, L J
Producer:
19990930
In:
Digestive diseases and sciences
vol. 44
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9.
The periodic paralyses.
[electronic resource]
by
Griggs, R C
Ptácek, L J
Producer:
19921215
In:
Hospital practice (Office ed.)
vol. 27
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10.
Channelopathies: episodic disorders of the nervous system.
[electronic resource]
by
Ptacek, L J
Fu, Y H
Producer:
20020327
In:
Epilepsia
vol. 42 Suppl 5
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11.
Chronic fatigue syndrome and channelopathies.
[electronic resource]
by
Waxman, S G
Ptacek, L J
Producer:
20010222
In:
Medical hypotheses
vol. 55
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12.
Mutations of sodium channels in periodic paralysis: can they explain the disease and predict treatment?
[electronic resource]
by
Griggs, R C
Ptácek, L J
Producer:
19990517
In:
Neurology
vol. 52
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13.
Anesthetic management of familial hypokalemic periodic paralysis during parturition.
[electronic resource]
by
Viscomi, C M
Ptacek, L J
Dudley, D
Producer:
19990520
In:
Anesthesia and analgesia
vol. 88
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14.
Genetics and physiology of the myotonic muscle disorders.
[electronic resource]
by
Ptacek, L J
Johnson, K J
Griggs, R C
Producer:
19930218
In:
The New England journal of medicine
vol. 328
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15.
Novel insights from genetic and molecular characterization of the human clock.
[electronic resource]
by
Ptácek, L J
Jones, C R
Fu, Y-H
Producer:
20080801
In:
Cold Spring Harbor symposia on quantitative biology
vol. 72
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16.
Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapy.
[electronic resource]
by
Jackson, C E
Barohn, R J
Ptacek, L J
Producer:
19940719
In:
Muscle & nerve
vol. 17
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17.
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family.
[electronic resource]
by
Sansone, V
Rotondo, G
Ptacek, L J
Meola, G
Producer:
19950525
In:
Italian journal of neurological sciences
vol. 15
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18.
Fetal anticonvulsant drug exposure: a population based study.
[electronic resource]
by
Robertson, L D
Swaiman, K F
Ptacek, L J
Producer:
19870121
In:
Neurotoxicology
vol. 7
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19.
Auditory clicks in extinction of stroboscope-induced seizures.
[electronic resource]
by
Forster, F M
Ptacek, L J
Peterson, W G
Producer:
19660108
In:
Epilepsia
vol. 6
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20.
Episodic movement disorders as channelopathies.
[electronic resource]
by
Bhatia, K P
Griggs, R C
Ptácek, L J
Producer:
20001002
In:
Movement disorders : official journal of the Movement Disorder Society
vol. 15
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