Atypical parkinsonian syndromes: a general neurologist’s perspective

le Deutschländer, A. B., Ross, O. A., Dickson, D. W., Wszolek, Z. K.
Foilsithe in Eur J Neurol (2017)

Essential tremor: predictors of disease progression in a clinical cohort

le Putzke, J D, Whaley, N R, Baba, Y, Wszolek, Z K, Uitti, R J
Foilsithe 2006

Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): A single entity?

le Wider, C, Van Gerpen, J A., DeArmond, S, Shuster, E A., Dickson, D W., Wszolek, Z K.
Foilsithe 2009

Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids

le Van Gerpen, J A., Wider, C, Broderick, D F., Dickson, D W., Brown, L A., Wszolek, Z K.
Foilsithe 2008

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation

le Konno, T., Yoshida, K., Mizuno, T., Kawarai, T., Tada, M., Nozaki, H., Ikeda, S.‐I., Nishizawa, M., Onodera, O., Wszolek, Z. K., Ikeuchi, T.
Foilsithe in Eur J Neurol (2016)

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.

le Gasser, T, Müller-Myhsok, B, Supala, A, Zimmer, E, Wieditz, G, Wszolek, Z K, Vieregge, P, Bonifati, V, Oertel, W H
Foilsithe 1996

A novel approach to dementia: High-resolution (1)H MRI of the human hippocampus performed at 21.1 T

le Schweitzer, K.J., Foroutan, P., Dickson, D.W., Broderick, D.F., Klose, U., Berg, D., Wszolek, Z.K., Grant, S.C.
Foilsithe 2010

Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

le DeJesus-Hernandez, M., Desaro, P., Johnston, A., Ross, O.A., Wszolek, Z.K., Ertekin-Taner, N., Graff-Radford, N.R., Rademakers, R., Boylan, K.
Foilsithe 2011

Progression of dopaminergic dysfunction in a LRRK2 kindred: A multitracer PET study

le Nandhagopal, R, Mak, E, Schulzer, M, McKenzie, J, McCormick, S, Sossi, V, Ruth, T J., Strongosky, A, Farrer, M J., Wszolek, Z K., Stoessl, A J.
Foilsithe 2008

MEIS1 p.R272H IN FAMILIAL RESTLESS LEGS SYNDROME

le Vilariño-Güell, C, Chai, H, Keeling, B H., Young, J E., Rajput, A, Lynch, T, Aasly, J O., Uitti, R J., Wszolek, Z K., Farrer, M J., Lin, S -C.
Foilsithe 2009

Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN

le Whitwell, J L., Jack, C R., Boeve, B F., Senjem, M L., Baker, M, Rademakers, R, Ivnik, R J., Knopman, D S., Wszolek, Z K., Petersen, R C., Josephs, K A.
Foilsithe 2009

Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations

le Whitwell, J L., Jack, C R., Boeve, B F., Senjem, M L., Baker, M, Ivnik, R J., Knopman, D S., Wszolek, Z K., Petersen, R C., Rademakers, R, Josephs, K A.
Foilsithe 2009

MRS in presymptomatic MAPT mutation carriers: A potential biomarker for tau-mediated pathology

le Kantarci, K., Boeve, B.F., Wszolek, Z.K., Rademakers, R., Whitwell, J.L., Baker, M.C., Senjem, M.L., Samikoglu, A.R., Knopman, D.S., Petersen, R.C., Jack, C.R.
Foilsithe 2010

Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN

le Whitwell, J.L., Weigand, S.D., Gunter, J.L., Boeve, B.F., Rademakers, R., Baker, M., Knopman, D.S., Wszolek, Z.K., Petersen, R.C., Jack, C.R., Josephs, K.A.
Foilsithe 2011

Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia

le Konno, T., Broderick, D.F., Mezaki, N., Isami, A., Kaneda, D., Tashiro, Y., Tokutake, T., Keegan, B.M., Woodruff, B.K., Miura, T., Nozaki, H., Nishizawa, M., Onodera, O., Wszolek, Z.K., Ikeuchi, T.
Foilsithe in AJNR Am J Neuroradiol (2017)

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy

le Vilariño-Güell, C., Soto-Ortolaza, A.I., Rajput, A., Mash, D.C., Papapetropoulos, S., Pahwa, R., Lyons, K.E., Uitti, R.J., Wszolek, Z.K., Dickson, D.W., Farrer, M.J., Ross, O.A.
Foilsithe 2011

A family with parkinsonism, essential tremor, restless legs syndrome, and depression

le Puschmann, A., Pfeiffer, R.F., Stoessl, A.J., Kuriakose, R., Lash, J.L., Searcy, J.A., Strongosky, A.J., Vilariño-Güell, C., Farrer, M.J., Ross, O.A., Dickson, D.W., Wszolek, Z.K.
Foilsithe 2011

Association of the MAPT locus with Parkinson’s disease

le Wider, C., Vilariño-Güell, C., Jasinska-Myga, B., Heckman, M. G., Soto-Ortolaza, A. I., Cobb, S. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Foilsithe 2009

Altered functional connectivity in asymptomatic MAPT subjects: A comparison to bvFTD

le Whitwell, J.L., Josephs, K.A., Avula, R., Tosakulwong, N., Weigand, S.D., Senjem, M.L., Vemuri, P., Jones, D.T., Gunter, J.L., Baker, M., Wszolek, Z.K., Knopman, D.S., Rademakers, R., Petersen, R.C., Boeve, B.F., Jack, C.R.
Foilsithe 2011

AN INDEPENDENT REPLICATION OF PARK16 IN ASIAN SAMPLES

le Vilariño-Güell, C., Ross, O.A., Aasly, J.O., White, L.R., Rajput, A., Rajput, A.H., Lynch, T., Krygowska-Wajs, A., Jasinska-Myga, B., Opala, G., Barcikowska, M., Lee, M.-C., Hentati, F., Uitti, R.J., Wszolek, Z.K., Farrer, M.J., Wu, R.-M.
Foilsithe 2010