The grasp and other primitive reflexes

Por Schott, J, Rossor, M
Publicado em 2003

Handedness among surgeons.

Por Schott, J., Puttick, M.
Publicado em 1995

Magnetic resonance imaging in dementia

Por Schott, J., Fox, N., Waldman, A.
Publicado em 2002

GENETICS OF THE DEMENTIAS

Por Schott, J, Fox, N, Rossor, M
Publicado em 2002

The Fe(2+)-His(F8) Raman band shape of deoxymyoglobin reveals taxonomic conformational substates of the proximal linkage.

Por Schott, J, Dreybrodt, W, Schweitzer-Stenner, R
Publicado em 2001

Development of selective verbal memory impairment secondary to a left thalamic infarct: a longitudinal case study

Por Schott, J, Crutch, S, Fox, N, Warrington, E
Publicado em 2003

Phenotypical variation in Alzheimer's disease: insights from posterior cortical atrophy

Por Slattery, C F, Crutch, S J, Schott, J M
Publicado no Pract Neurol (2015)

Transient ischaemic attacks are associated with increased rates of global cerebral atrophy

Por Walters, R, Fox, N, Schott, J, Crum, W, Stevens, J, Rossor, M, Thomas, D
Publicado em 2003

Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy

Por Paviour, D, Schott, J, Stevens, J, Revesz, T, Holton, J, Rossor, M, Lees, A, Fox, N
Publicado em 2004

Reduced sample sizes for atrophy outcomes in Alzheimer's disease trials: baseline adjustment

Por Schott, J.M., Bartlett, J.W., Barnes, J., Leung, K.K., Ourselin, S., Fox, N.C.
Publicado em 2010

Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration

Por Janssen, J, Schott, J, Cipolotti, L, Fox, N, Scahill, R, Josephs, K, Stevens, J, Rossor, M
Publicado em 2005

Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1

Por Le Caignec, C., Lefevre, M., Schott, J. J., Chaventre, A., Gayet, M., Calais, C., Moisan, J. P.
Publicado em 2002

Protein dynamics in an intermediate state of myoglobin: optical absorption, resonance Raman spectroscopy, and x-ray structure analysis.

Por Engler, N, Ostermann, A, Gassmann, A, Lamb, D C, Prusakov, V E, Schott, J, Schweitzer-Stenner, R, Parak, F G
Publicado em 2000

Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

Por Pravenec, M, Gauguier, D, Schott, J J, Buard, J, Kren, V, Bila, V, Szpirer, C, Szpirer, J, Wang, J M, Huang, H
Publicado em 1995

Cerebrospinal fluid markers including trefoil factor 3 are associated with neurodegeneration in amyloid-positive individuals

Por Paterson, R W, Bartlett, J W, Blennow, K, Fox, N C, Shaw, L M, Trojanowski, J Q, Zetterberg, H, Schott, J M
Publicado em 2014

Biomarkers in dementia: clinical utility and new directions

Por Ahmed, R M, Paterson, R W, Warren, J D, Zetterberg, H, O'Brien, J T, Fox, N C, Halliday, G M, Schott, J M
Publicado no J Neurol Neurosurg Psychiatry (2014)

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Por Duval, D., Lardeux, A., Le Tourneau, T., Norris, R.A., Markwald, R.R., Sauzeau, V., Probst, V., Le Marec, H., Levine, R., Schott, J.J., Merot, J.
Publicado em 2013

CSF biomarkers for Alzheimer's pathology and the effect size of APOE ɛ4

Por Andreasson, U, Lautner, R, Schott, J M, Mattsson, N, Hansson, O, Herukka, S-K, Helisalmi, S, Ewers, M, Hampel, H, Wallin, A, Minthon, L, Hardy, J, Blennow, K, Zetterberg, H
Publicado em 2014

Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

Por Kyndt, F, Schott, J J, Trochu, J N, Baranger, F, Herbert, O, Scott, V, Fressinaud, E, David, A, Moisan, J P, Bouhour, J B, Le Marec, H, Bénichou, B
Publicado em 1998

The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.

Por Lubianca Neto, J F, Lu, L, Eavey, R D, Flores, M A, Caldera, R M, Sangwatanaroj, S, Schott, J J, McDonough, B, Santos, J I, Seidman, C E, Seidman, J G
Publicado em 1998