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Results of search for 'au:"SULLIVAN, A A"'
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Authors
Albin, R L
Allworth, A M
BARE, W W
Benson, S M
Boyle, R
Boyle, R S
Chervin, R D
Chuah, T L
Csurhes, P A
Curtain, R
Ewart, A H
Fanning, S F
Farnebo, F
Flanagan, S
Green, K
Larsson, C
Schalling, M
Sullivan, A A
Teh, B T
Whitby, R M
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Topics
Adolescent
Adult
Aged
Australia
Dementia, Multi-Infarct
Female
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Pedigree
Proto-Oncogene Proteins
Receptor, Notch3
Receptors, Cell Surface
Receptors, Notch
adverse effects
complications
etiology
genetics
pathology
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English
Your search returned 10 results.
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1.
Comparison of intravenous saccharated iron oxide and whole blood in treatment of hypochromic anemia of pregnancy.
[electronic resource]
by
BARE, W W
SULLIVAN, A A
Producer:
19981101
In:
American journal of obstetrics and gynecology
vol. 79
Online resources:
Available from publisher's website
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No items available.
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2.
Vaccine-associated paralytic poliomyelitis.
[electronic resource]
by
Sullivan, A A
Boyle, R S
Whitby, R M
Producer:
19951130
In:
The Medical journal of Australia
vol. 163
Online resources:
Available from publisher's website
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No items available.
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3.
Perianal zygomycosis in paroxysmal nocturnal haemoglobinuria.
[electronic resource]
by
Fanning, S F
Sullivan, A A
Allworth, A M
Producer:
19930223
In:
Australian and New Zealand journal of medicine
vol. 22
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No items available.
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4.
Parkinsonism after correction of hyponatremia with radiological central pontine myelinolysis and changes in the basal ganglia.
[electronic resource]
by
Sullivan, A A
Chervin, R D
Albin, R L
Producer:
20000815
In:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
vol. 7
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5.
Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigree.
[electronic resource]
by
Grigg, R
Lea, R
Sullivan, A A
Curtain, R
MacMillian, J
Griffiths, L
Producer:
20001121
In:
Human mutation
vol. 16
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6.
T cell reactivity to P0, P2, PMP-22, and myelin basic protein in patients with Guillain-Barre syndrome and chronic inflammatory demyelinating polyradiculoneuropathy.
[electronic resource]
by
Csurhes, P A
Sullivan, A-A
Green, K
Pender, M P
McCombe, P A
Producer:
20051020
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 76
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7.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.
[electronic resource]
by
Sullivan, A A
Teh, B T
Jeavons, S
Schalling, M
Silburn, P
Larsson, C
Boyle, R
Producer:
20100203
In:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
vol. 4
Online resources:
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8.
Cerebral histoplasmosis in an Australian patient with systemic lupus erythematosus.
[electronic resource]
by
Sullivan, A A
Benson, S M
Ewart, A H
Hogan, P G
Whitby, R M
Boyle, R S
Producer:
19980916
In:
The Medical journal of Australia
vol. 169
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9.
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred.
[electronic resource]
by
Teh, B T
Sullivan, A A
Farnebo, F
Zander, C
Li, F Y
Strachan, N
Schalling, M
Larsson, C
Sandstrom, P
Producer:
19970616
In:
Clinical genetics
vol. 51
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10.
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.
[electronic resource]
by
Chuah, T L
Tan, K M
Tan, S M
Flanagan, S
Hyland, V
Sullivan, A A
Henderson, R
MacMillan, J
Lander, C
Producer:
20011207
In:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
vol. 8
Online resources:
Available from publisher's website
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