α-Synuclein Locus Triplication Causes Parkinson's Disease von Singleton, A. B., Farrer, M., Johnson, J., Singleton, A., Hague, S., Kachergus, J., Hulihan, M., Peuralinna, T., Dutra, A., Nussbaum, R., Lincoln, S., Crawley, A., Hanson, M., Maraganore, D., Adler, C., Cookson, M. R., Muenter, M., Baptista, M., Miller, D., Blancato, J., Hardy, J., Gwinn-Hardy, K.

Volltext

The impact of chelation therapy on survival in transfusional iron overload: a meta‐analysis of myelodysplastic syndrome von Mainous, Arch G., Tanner, Rebecca J., Hulihan, Mary M., Amaya, Mirna, Coates, Thomas D.

Volltext

LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study von Hulihan, Mary M, MPH, Ishihara-Paul, Lianna, PhD, Kachergus, Jennifer, BSc, Warren, Liling, PhD, Amouri, Rim, PhD, Elango, Ramu, PhD, Prinjha, Rab K, PhD, Upmanyu, Ruchi, MSc, Kefi, Mounir, MD, Zouari, Mourad, MD, Sassi, Samia Ben, MD, Yahmed, Samia Ben, MD, El Euch-Fayeche, Ghada, MD, Matthews, Paul M, PhD, Middleton, Lefkos T, MD, Gibson, Rachel A, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, PhD

Volltext

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication von FUCHS, J, NILSSON, C, GASSER, T, FARRER, M. J, KACHERGUS, J, MUNZ, M, LARSSON, E.-M, SCHÜLE, B, LANGSTON, J. W, MIDDLETON, F. A, ROSS, O. A, HULIHAN, M

Volltext

PINK1 mutations and parkinsonism von ISHIHARA-PAUL, L, HULIHAN, M. M, ZOUARI, M, SASSI, S. B, YAHMED, S. B, EL EUCH-FAYECHE, G, MATTHEWS, P. M, MIDDLETON, L. T, GIBSON, R. A, HENTATI, F, FARRER, M. J, KACHERGUS, J, UPMANYU, R, WARREN, L, AMOURI, R, ELANGO, R, PRINJHA, R. K, SOTO, A, KEFI, M

Volltext

Lrrk2 pathogenic substitutions in Parkinson's disease von MATA, Ignacio F, KACHERGUS, Jennifer M, LAHOZ, Carlos, WSZOLEK, Zbigniew K, FARRER, Matthew J, TAYLOR, Julie P, LINCOLN, Sarah, AASLY, Jan, LYNCH, Timothy, HULIHAN, Mary M, COBB, Stephanie A, WU, Ruey-Meei, LU, Chin-Song

Volltext

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia von Farrer, Matthew J, Stone, Jeremy T, Lin, Chin-Hsien, Dächsel, Justus C, Hulihan, Mary M, Haugarvoll, Kristoffer, Ross, Owen A, Wu, Ruey-Meei

Volltext

278 Emergency Department Utilization by Californians With Sickle Cell Disease, 2005-2014 von Paulukonis, S, Vichinsky, E, Neumayr, L, Treadwell, M, Coates, T, Feuchtbaum, L, Hulihan, M

Volltext

Public Health Surveillance of Nonmalignant Blood Disorders von Beckman, Michele G., MPH, Hulihan, Mary M., MPH, Byams, Vanessa R., MPH, Oakley, Meredith A., DVM, MPH, Reyes, Nimia, MD, Trimble, Sean, MPH, Grant, Althea M., PhD, MPH

Volltext

LRRK2 mutations in Parkinson disease von FARRER, M, STONE, J, MATA, I. F, LINCOLN, S, KACHERGUS, J, HULIHAN, M, STRAIN, K. J, MARAGANORE, D. M

Volltext

Characterization of DCTN1 genetic variability in neurodegeneration von VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

Volltext

Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians von Shokar, Navkiran K., Baker, Richard, Harle, Christopher A., Tanner, Rebecca J., Mainous, Arch G., Hulihan, Mary M.

Volltext

Transferrin Saturation and Hospital Length of Stay and Mortality in Medicare Beneficiaries von Mainous III, Arch G., Diaz, Vanessa A., Knoll, Michele E., Hulihan, Mary M., Grant, Althea M., Wright, Robert U.

Volltext

Lrrk2 R1441 substitution and progressive supranuclear palsy von Ross, O. A., Whittle, A. J., Cobb, S. A., Hulihan, M. M., Lincoln, S. J., Toft, M., Farrer, M. J., Dickson, D. W.

Volltext

Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008 von Paulukonis, Susan T., Eckman, James R., Snyder, Angela B., Hagar, Ward, Feuchtbaum, Lisa B., Zhou, Mei, Grant, Althea M., Hulihan, Mary M.

Volltext

Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiv... von Badawy, Sherif M., Payne, Amanda B., Hulihan, Mary M., Coates, Thomas D., Majumdar, Suvankar, Smith, Dominic, Thompson, Alexis A.

Volltext

Genomic investigation of α-synuclein multiplication and parkinsonism von Ross, Owen A., Braithwaite, Adam T., Skipper, Lisa M., Kachergus, Jennifer, Hulihan, Mary M., Middleton, Frank A., Nishioka, Kenya, Fuchs, Julia, Gasser, Thomas, Maraganore, Demetrius M., Adler, Charles H., Larvor, Lydie, Chartier-Harlin, Marie-Christine, Nilsson, Christer, Langston, J. William, Gwinn, Katrina, Hattori, Nobutaka, Farrer, Matthew J.

Volltext

DCTN1 mutations in Perry syndrome von Farrer, Matthew J, Hulihan, Mary M, Kachergus, Jennifer M, Dächsel, Justus C, Stoessl, A Jon, Grantier, Linda L, Calne, Susan, Calne, Donald B, Lechevalier, Bernard, Chapon, Francoise, Tsuboi, Yoshio, Yamada, Tatsuo, Gutmann, Ludwig, Elibol, Bülent, Bhatia, Kailash P, Wider, Christian, Vilariño-Güell, Carles, Ross, Owen A, Brown, Laura A, Castanedes-Casey, Monica, Dickson, Dennis W, Wszolek, Zbigniew K

Volltext

Emergency department utilization by Californians with sickle cell disease, 2005–2014 von Paulukonis, Susan T., Feuchtbaum, Lisa B., Coates, Thomas D., Neumayr, Lynne D., Treadwell, Marsha J., Vichinsky, Elliott P., Hulihan, Mary M.

Volltext

The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia von Grosse, Scott D., Boulet, Sheree L., Grant, Althea M., Hulihan, Mary M., Faughnan, Marie E.

Volltext