Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Irfan Lalani"'
Autor:
Teepu Siddique, Albert J. Tahmoush, Faisal Fecto, Irfan Lalani, Han Xiang Deng, Kaouther Ajroud, Vamsi K. Mootha, Sarah E. Calvo, Senda Ajroud-Driss, Terry Heiman-Patterson, Nailah Siddique
Publikováno v:
neurogenetics. 16:1-9
Mitochondrial myopathies belong to a larger group of systemic diseases caused by morphological or biochemical abnormalities of mitochondria. Mitochondrial disorders can be caused by mutations in either the mitochondrial or nuclear genome. Only 5 % of
Autor:
Bernard M. Abrams, Meredith C.B. Adams, Ashley Agerson, Dustin Anderson, Magdalena Anitescu, A. Vania Apkarian, Charles E. Argoff, Juan Francisco Asenjo, John A. Bailey, Stephen J. Bekanich, Benoy Benny, Honorio T. Benzon, Klaus Bielefeldt, Brian Birmingham, Michael M. Bottros, Randall P. Brewer, Jason C. Brookman, David L. Brown, Chad M. Brummett, Kim J. Burchiel, Allen W. Burton, Asokumar Buvanendran, Alex Cahana, Kenneth D. Candido, James Celestin, Kwai-Tung Chan, Ronil V. Chandra, Kailash Chandwani, Delia Chiaramonte, Roger Chou, Daniel Clauw, Steven P. Cohen, David Copenhaver, Megan H. Cortazzo, Edward C. Covington, Nessa Coyle, Chris D'Adamo, Carlton Dampier, Miles Day, Oscar de Leon-Casasola, Andrew Dubin, Michael A. Erdek, Vania E. Fernandez, Perry G. Fine, Scott M. Fishman, Julie S. Franklin, Timothy Furnish, Vicente Garcia Tomas, Robert J. Gatchel, G.F. Gebhart, Myra Glajchen, Michael Gofeld, Rachael Gooberman-Hill, Andrew H. Gordon, Martin Grabois, Carmen R. Green, Anil Gupta, Admir Hadzic, Robbie Haggard, Marie N. Hanna, R. Norman Harden, Simon Haroutiunian, Richard L. Harvey, Alicia Heapy, Omar H. Henriquez, Joshua A. Hirsch, Marc A. Huntoon, Robert W. Hurley, Mohammed Issa, Kenneth C. Jackson, Benjamin W. Johnson, Leonardo Kapural, Robert D. Kerns, Farooq Khan, Amy J. Kirsling, Kanupriya Kumar, Kwesi Kwofie, Irfan Lalani, Jennifer M. Lee, Thabele M. Leslie-Mazwi, Yuan-Chi Lin, Matthew J.P. LoDico, Khalid Malik, Asha Manohar, Edward R. Mariano, Timothy P. Maus, Gary McCleane, Brian E. McGeeney, Noshir R. Mehta, Sonal Mehta, Douglas G. Merrill, Harold Merskey, James R. Miner, Brian Morrison, Geeta Nagpal, Patrick Narchi, Joseph M. Neal, Barry Nicholls, Lone Nikolajsen, Jean-Pierre P. Ouanes, Xavier Paqueron, Sagar S. Parikh, Winston C.V. Parris, Meenal Patil, Frederick M. Perkins, David A. Provenzano, James D. Rabinov, Mohammed Ranavaya, Ahmed M. Raslan, James P. Rathmell, M. Cary Reid, W. Evan Rivers, Robert D. Rondinelli, Marta J. Rozanski, Francis V. Salinas, Emine Aysu Salviz, Amod Sawardekar, Pat Schofield, Steven J. Scrivani, Elizabeth Seng, Ravi Shah, Hariharan Shankar, Vandana Sharma, Uma Shastri, Stephen D. Silberstein, François Singelyn, Howard S. Smith, Melanie B. Smith, Egilius L.H. Spierings, Jeanette S. Springer, Steven P. Stanos, Carrie Stewart, Santhanam Suresh, David Tauben, Gregory W. Terman, Brian R. Theodore, Katrina M. Thomas, Knox H. Todd, Dennis C. Turk, Mark D. Tyburski, Meredith G. van der Velden, Maarten van Eerd, Maarten van Kleef, Jan Van Zundert, Renata Variakojis, Jeanine A. Verbunt, Thomas R. Vetter, David B. Waisel, Howard J. Waldman, Mark S. Wallace, Ajay D. Wasan, Karin N. Westlund, Harriët M. Wittink, Christopher L. Wu, Daquan Xu, Tony L. Yaksh, Robert P. Yezierski, Albert J. Yoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a15c5a45cef8284f9468f7f271e6ef76
https://doi.org/10.1016/b978-0-323-08340-9.01002-1
https://doi.org/10.1016/b978-0-323-08340-9.01002-1
Publikováno v:
Journal of Neuroimaging. 16:364-366
The clinical syndrome of tuberculous (TB) meningitis leading to ischemic strokes is rarely seen today in immunocompetent adults native to North America. This entity is also notoriously difficult to diagnose because the presenting symptoms are often n
Autor:
Bernard M. Abrams, A.V. Apkarian, Charles E. Argoff, Kjell Axelsson, Mani Batra, Benoy Benny, Honorio T. Benzon, Klaus Bielefeldt, David M. Biondi, Hemmo Bosscher, Randall P. Brewer, David L. Brown, Chad M. Brummett, Allen W. Burton, Asokumar Buvanendran, Alex Cahana, Kenneth D. Candido, David Casarett, Kwai-Tung Chan, Susan L. Charette, Steven P. Cohen, Megan H. Cortazzo, Edward C. Covington, Nessa Coyle, Timothy R. Deer, Oscar de Leon-Casasola, Bonnie Deschner, Robert H. Dworkin, Michael Erdek, Bruce A. Ferrell, Perry G. Fine, Scott M. Fishman, Kenneth A. Follett, G.F. Gebhart, Shiv K. Goel, Martin Grabois, Brock Gretter, Anil Gupta, Admir Hadzic, Naeem Haider, Alicia Heapy, James E. Heavner, Matthew D. Hepler, Marc A. Huntoon, Robert W. Hurley, Kenneth C. Jackson, Benjamin Johnson, Robert D. Kerns, Timothy L. Lacy, Irfan Lalani, Thomas M. Larkin, Elaina E. Lin, Yuan-Chi Lin, Spencer S. Liu, Raymond Maciewicz, David N. Maine, Khalid Malik, Timothy P. Maus, Brenda C. McClain, Gary McCleane, Brian McGeeney, Nashir R. Mehta, Nagy Mekhail, Douglas G. Merrill, Harold Merskey, Marjorie Meyer, James R. Miner, Beth H. Minzter, Robert E. Molloy, Antoun Nader, Patrick Narchi, Joseph M. Neal, Krystof J. Neumann, Jon B. Obray, Marco Pappagallo, Xavier Paqueron, Winston C.V. Parris, Fred Perkins, Sudhir Rao, James P. Rathmell, Scott S. Reuben, Christopher Robards, Richard W. Rosenquist, I.Jon Russell, Francis V. Salinas, Michael D. Sather, Michael F. Schafer, Steven J. Scrivani, Stelian Serban, Stephen D. Silberstein, François Singelyn, Menno Sluijter, Amol Soin, Steven P. Stanos, Santhanam Suresh, Kimberly S. Swanson, Sally Tarbell, Knox H. Todd, Dennis C. Turk, Mark D. Tyburski, M.van Kleef, J.Van Zundert, Renata Variakojis, Jeanine A. Verbunt, Christopher M. Viscomi, Mitchell Wachtel, Howard J. Waldman, David Walega, Daniel T. Warren, Tabitha Washington, Karin N. Westlund High, Brian A. Willams, Kayode A. Williams, Harrië Wittink, Christopher L. Wu, Daquan Xu, Tony L. Yaksh, Anthony Yarussi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76e25909f303b0f5cdf1d9e19f1279e7
https://doi.org/10.1016/b978-032304184-3.50001-7
https://doi.org/10.1016/b978-032304184-3.50001-7
Autor:
Irfan Lalani
Publikováno v:
Neurology. 67(8)
Traditionally neurologists have been considered masterful diagnosticians. Fellow physicians often rely on neurologists to sort out complex historical and examination data in order to arrive at a diagnosis and plan of action. Our specialty is also kno
Autor:
Wu Yen Hung, Rim Amouri, Teepu Siddique, Irfan Lalani, Karim Ouahchi, Samir Belal, Ghada El Euch-Fayache, Fayçal Hentati, Ilhem Turki
Publikováno v:
Archives of neurology. 60(7)
Background Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a clinically homogenous disorder reported in Quebec caused by mutations in the SACS gene (chromosome 13q12). Recently, we identified a Tunisian kindred demonstrating lin
Autor:
Teepu, Siddique, Irfan, Lalani
Publikováno v:
Advances in neurology. 88
Publikováno v:
Pediatric Neurology. 36:64-65
There is a wide differential diagnosis for patients presenting with multiple cranial nerve palsies, including infectious, inflammatory, malignant, genetic, toxic, and metabolic conditions. This report describes the clinical features, neuroimaging fin