Chronic Allergic Inflammation Causes Vascular Remodeling and Pulmonary Hypertension in Bmpr2 Hypomorph and Wild-Type Mice

Por Mushaben, Elizabeth M., Hershey, Gurjit Khurana, Pauciulo, Michael W., Nichols, William C., Le Cras, Timothy D.
Publicado em 2012

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

Por Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana
Publicado em 2010

Alpha-Synuclein and Familial Parkinson’s Disease

Por Pankratz, Nathan, Nichols, William C., Elsaesser, Veronika E., Pauciulo, Michael W., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Pfeiffer, Ronald F., Foroud, Tatiana
Publicado em 2009

Mutations in DJ-1 are rare in familial Parkinson disease

Por Pankratz, Nathan, Pauciulo, Michael W., Elsaesser, Veronika E., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Shults, Clifford W., Foroud, Tatiana, Nichols Ph.D., William C.
Publicado em 2006

High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension

Por Sundaram, Nambirajan, Tailor, Anitaben, Mendelsohn, Laurel, Wansapura, Janaka, Wang, Xunde, Higashimoto, Tomoyasu, Pauciulo, Michael W., Gottliebson, William, Kalra, Vijay K., Nichols, William C., Kato, Gregory J., Malik, Punam
Publicado em 2010

High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension

Por Cogan, Joy D., Pauciulo, Michael W., Batchman, Amy P., Prince, Melissa A., Robbins, Ivan M., Hedges, Lora K., Stanton, Krista C., Wheeler, Lisa A., Phillips, John A., Loyd, James E., Nichols, William C.
Publicado em 2006

Genetic and Clinical Predictors of Deep Brain Stimulation in Young‐Onset Parkinson's Disease

Por Pal, Gian D., Hall, Deborah, Ouyang, Bichun, Phelps, Jessica, Alcalay, Roy, Pauciulo, Michael W., Nichols, William C., Clark, Lorraine, Mejia‐Santana, Helen, Blasucci, Lucia, Goetz, Christopher G., Comella, Cynthia, Colcher, Amy, Gan‐Or, Ziv, Rouleau, Guy A., Marder, Karen
Publicado no Mov Disord Clin Pract (2016)

Glucocerebrosidase activity in Parkinson’s disease with and without GBA mutations

Por Alcalay, Roy N., Levy, Oren A., Waters, Cheryl C., Fahn, Stanley, Ford, Blair, Kuo, Sheng-Han, Mazzoni, Pietro, Pauciulo, Michael W., Nichols, William C., Gan-Or, Ziv, Rouleau, Guy A., Chung, Wendy K., Wolf, Pavlina, Oliva, Petra, Keutzer, Joan, Marder, Karen, Zhang, Xiaokui
Publicado no Brain (2015)

BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

Por Machado, Rajiv D, Pauciulo, Michael W., Thomson, Jennifer R., Lane, Kirk B., Morgan, Neil V., Wheeler, Lisa, Phillips III, John A., Newman, John, Williams, Denise, Galiè, Nazzareno, Manes, Alessandra, McNeil, Keith, Yacoub, Magdi, Mikhail, Ghada, Rogers, Paula, Corris, Paul, Humbert, Marc, Donnai, Dian, Martensson, Gunnar, Tranebjaerg, Lisbeth, Loyd, James E., Trembath, Richard C., Nichols, William C.
Publicado em 2001