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Search Results - Leijenaar, Jolien F.
Search Results - Leijenaar, Jolien F.
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Methylphenidate and galantamine in patients with vascular cognitive impairment-the proof-of-principle study STREAM-VCI
by
Leijenaar, Jolien F
,
Groeneveld, Geert Jan
,
Klaassen, Erica S
,
Leeuwis, Anna E
,
Scheltens, Philip
,
Weinstein, Henry C
,
van Gerven, Joop M A
,
Barkhof, Frederik
,
van der Flier, Wiesje M
,
Prins, Niels D
Published in
Alzheimer's research & therapy
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Lower cerebral blood flow in subjects with Alzheimer's dementia, mild cognitive impairment, and subjective cognitive decline using two-dimensional phase-contrast magnetic resonance...
by
Leijenaar, Jolien F.
,
van Maurik, Ingrid S.
,
Kuijer, Joost P.A.
,
van der Flier, Wiesje M.
,
Scheltens, Philip
,
Barkhof, Frederik
,
Prins, Niels D.
Published in
Alzheimer's & dementia : diagnosis, assessment & disease monitoring
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Effect of magnesium treatment and glucose levels on delayed cerebral ischemia in patients with subarachnoid hemorrhage: a substudy of the Magnesium in Aneurysmal Subarachnoid Haemo...
by
Leijenaar, Jolien F.
,
Mees, Sanne M. Dorhout
,
Algra, Ale
,
Van Den Bergh, Walter M.
,
Rinkel, Gabriel J. E.
Published in
International journal of stroke
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From corticocentrism to leucocentrism or both
by
Leijenaar, Jolien F.
,
Scheltens, Philip
Published in
Brain (London, England : 1878)
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Nemaline myopathy caused by TNNT1 mutations in a Dutch pedigree
by
Pol, W. Ludo
,
Leijenaar, Jolien F.
,
Spliet, Wim G. M.
,
Lavrijsen, Selma W.
,
Jansen, Nicolaas J. G.
,
Braun, Kees P. J.
,
Mulder, Marcel
,
Timmers‐Raaijmakers, Brigitte
,
Ratsma, Kimberly
,
Dooijes, Dennis
,
Haelst, Mieke M.
Published in
Molecular genetics & genomic medicine
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Nemaline myopathy caused by TNNT1 mutations in a D utch pedigree
by
van der Pol, W. Ludo
,
Leijenaar, Jolien F.
,
Spliet, Wim G. M.
,
Lavrijsen, Selma W.
,
Jansen, Nicolaas J. G.
,
Braun, Kees P. J.
,
Mulder, Marcel
,
Timmers‐Raaijmakers, Brigitte
,
Ratsma, Kimberly
,
Dooijes, Dennis
,
van Haelst, Mieke M.
Published in
Molecular genetics & genomic medicine
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Nemaline myopathy caused byTNNT1 mutations in a Dutch pedigree
by
van der Pol, W Ludo
,
Leijenaar, Jolien F
,
Spliet, Wim G M
,
Lavrijsen, Selma W
,
Jansen, Nicolaas J G
,
Braun, Kees P J
,
Mulder, Marcel
,
Timmers-Raaijmakers, Brigitte
,
Ratsma, Kimberly
,
Dooijes, Dennis
,
van Haelst, Mieke M
Published in
Molecular genetics & genomic medicine
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Molecular Genetics & Genomic Medicine
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Alzheimer's & Dementia : Diagnosis, Assessment & Disease Monitoring
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Alzheimer's & Dementia. Diagnosis, Assessment & Disease Monitoring
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Alzheimer's Research & Therapy
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Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
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International Journal Of Stroke
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Binswanger's Disease
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