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	1.	A case of hereditary inclusion body myopathy: 1 patient, 2 novel mutations. [electronic resource] by Fisher, Justin Towfighi, Javad Darvish, Daniel Simmons, Zachary Producer: 20121002 In: Journal of clinical neuromuscular disease vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	MTHFR C677T genotype frequency in patients of Middle Eastern descent as determined by real-time PCR and melting curve analysis. [electronic resource] by Haghighatgoo, Arman Valles-Ayoub, Yadira Saechao, Chai Esfandiarifard, Saghi Martinez, Sarah L Pietruszka, Marvin Darvish, Daniel Producer: 20091026 In: Genetic testing and molecular biomarkers vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Validation of GNE:p.M712T identification by melting curve analysis. [electronic resource] by Valles-Ayoub, Yadira Saechao, Chai Haghighatgoo, Arman Neshat, Mehran S Esfandiarifard, Saghi Pietruszka, Marvin Darvish, Daniel Producer: 20080612 In: Genetic testing vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry. [electronic resource] by Valles-Ayoub, Yadira Esfandiarifard, Saghi No, Daniel Sinai, Pedram Khokher, Zeshan Kohan, Melody Kahen, Tanaz Darvish, Daniel Producer: 20111003 In: Genetic testing and molecular biomarkers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Non-GNE Quadriceps Sparing Distal Myopathy in an Iranian Jewish Patient. [electronic resource] by Mishra, Shri K Valles-Ayoub, Yadira Darvish, Daniel Khosa, Shaweta Moheb, Negar Trikamji, Bhavesh Rafiei, Nastaran Freundlich, Robert Producer: 20191213 In: Journal of clinical neuromuscular disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy. [electronic resource] by Valles-Ayoub, Yadira Esfandiarifard, Saghi Sinai, Pedram Carbajo, Rosangela Khokher, Zeshan No, Daniel Pietruszka, Marvin Darvish, Babak Kakkis, Emil Darvish, Daniel Producer: 20121010 In: Genetic testing and molecular biomarkers vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Preclinical assessment of wt GNE gene plasmid for management of hereditary inclusion body myopathy 2 (HIBM2). [electronic resource] by Jay, Chris Nemunaitis, Gregory Nemunaitis, John Senzer, Neil Hinderlich, Stephan Darvish, Daniel Ogden, Julie Eager, John Tong, Alex Maples, Phillip B Producer: 20100520 In: Gene regulation and systems biology vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathy. [electronic resource] by Gottlieb, Emily Ciccone, Carla Darvish, Daniel Naiem-Cohen, Shahrouz Dalakas, Marinos C Savelkoul, Paul J Krasnewich, Donna M Gahl, William A Huizing, Marjan Producer: 20060123 In: Molecular genetics and metabolism vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. [electronic resource] by Watts, Giles D J Wymer, Jill Kovach, Margaret J Mehta, Sarju G Mumm, Steven Darvish, Daniel Pestronk, Alan Whyte, Michael P Kimonis, Virginia E Producer: 20040816 In: Nature genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Novel GNE mutations in autosomal recessive hereditary inclusion body myopathy patients. [electronic resource] by No, Daniel Valles-Ayoub, Yadira Carbajo, Rosangela Khokher, Zeshan Sandoval, Lucia Stein, Beth Tarnopolsky, Mark Andrew Mozaffar, Tahseen Darvish, Babak Pietruszka, Marvin Darvish, Daniel Producer: 20131030 In: Genetic testing and molecular biomarkers vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent. [electronic resource] by Saechao, Chai Valles-Ayoub, Yadira Esfandiarifard, Saghi Haghighatgoo, Arman No, Daniel Shook, Steven Mendell, Jerry R Rosales-Quintero, Xiomara Felice, Kevin J Morel, Chantal F Pietruska, Marvin Darvish, Daniel Producer: 20100729 In: Genetic testing and molecular biomarkers vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine. [electronic resource] by Galeano, Belinda Klootwijk, Riko Manoli, Irini Sun, MaoSen Ciccone, Carla Darvish, Daniel Starost, Matthew F Zerfas, Patricia M Hoffmann, Victoria J Hoogstraten-Miller, Shelley Krasnewich, Donna M Gahl, William A Huizing, Marjan Producer: 20070710 In: The Journal of clinical investigation vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	The Gne M712T mouse as a model for human glomerulopathy. [electronic resource] by Kakani, Sravan Yardeni, Tal Poling, Justin Ciccone, Carla Niethamer, Terren Klootwijk, Enriko D Manoli, Irini Darvish, Daniel Hoogstraten-Miller, Shelley Zerfas, Patricia Tian, E Ten Hagen, Kelly G Kopp, Jeffrey B Gahl, William A Huizing, Marjan Producer: 20120725 In: The American journal of pathology vol. 180 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Limb-girdle muscular dystrophy in the United States. [electronic resource] by Moore, Steven A Shilling, Christopher J Westra, Steven Wall, Cheryl Wicklund, Matthew P Stolle, Catherine Brown, Charlotte A Michele, Daniel E Piccolo, Federica Winder, Thomas L Stence, Aaron Barresi, Rita King, Nick King, Wendy Florence, Julaine Campbell, Kevin P Fenichel, Gerald M Stedman, Hansell H Kissel, John T Griggs, Robert C Pandya, Shree Mathews, Katherine D Pestronk, Alan Serrano, Carmen Darvish, Daniel Mendell, Jerry R Producer: 20061114 In: Journal of neuropathology and experimental neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)