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Ali, Naushin S.
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1

Mitigating Infection Risk in Upper Airway Stimulation:

Ali, Naushin S. ; Fitzpatrick IV, Thomas H. ; Islam, Albina S..
Annals of Otology, Rhinology & Laryngology.  133 (2023)  3 - p. 277-283 , 2023
Link: https://doi.org/10.1177/..
 
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2

511 Characteristics of Inhalation Injury Management at a Re..:

Drake, Mack ; Leichtle, Stefan ; Todd Borchers, C...
Journal of Burn Care & Research.  43 (2022)  Supplement_1 - p. S90-S91 , 2022
Link: https://doi.org/10.1093/..
 
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3

List of Contributors:

, In: Plant Signaling Molecules,
Raina, Aamir ; Banerjee, Aditya ; Kamal, Aisha... - p. xi-xiv , 2019
Link: https://doi.org/10.1016/..
 
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4

Doxycycline-Induced Intracranial Hypertension Presenting as..:

Ali, Naushin Shabnam ; Long, Barry Daniel ; Manzoor, Nauman F...
Otology & Neurotology Open.  3 (2023)  4 - p. e043 , 2023
Link: https://doi.org/10.1097/..
 
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5

An evaluation of overall effectiveness and treatment satisf..:

Sholapur, Naushin S. ; Hamilton, Korinne ; Butler, Lianna..
Transfusion.  56 (2016)  7 - p. 1739-1744 , 2016
Link: https://doi.org/10.1111/..
 
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6

Mutations in SPATA13/ASEF2 cause primary angle closure glau..:

Waseem, Naushin H. ; Low, Sancy ; Shah, Amna Z....
PLOS Genetics.  16 (2020)  4 - p. e1008721 , 2020
Link: https://doi.org/10.1371/..
 
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7

Genetic association and stress mediated down-regulation in ..:

Vishal, Mansi ; Sharma, Anchal ; Kaurani, Lalit...
BMC Medical Genomics.  9 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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8

Rare and common variants in extracellular matrix gene Fibri..:

Ratnapriya, Rinki ; Zhan, Xiaowei ; Fariss, Robert N....
Human Molecular Genetics.  23 (2014)  21 - p. 5827-5837 , 2014
Link: https://doi.org/10.1093/..
 
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9

A Homozygous Mutation in theTUBGene Associated with Retinal..:

Borman, Arundhati Dev ; Pearce, Laura R. ; Mackay, Donna S....
Human Mutation.  35 (2013)  3 - p. 289-293 , 2013
Link: https://doi.org/10.1002/..
 
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10

RP1L1Variants are Associated with a Spectrum of Inherited R..:

Davidson, Alice E. ; Sergouniotis, Panagiotis I. ; Mackay, Donna S....
Human Mutation.  34 (2013)  3 - p. 506-514 , 2013
Link: https://doi.org/10.1002/..
 
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11

NMNAT1 mutations cause Leber congenital amaurosis:

Falk, Marni J ; Zhang, Qi ; Nakamaru-Ogiso, Eiko...
Nature Genetics.  44 (2012)  9 - p. 1040-1045 , 2012
Link: https://doi.org/10.1038/..
 
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12

Expression of PRPF31 and TFPT: regulation in health and ret..:

Rose, Anna M. ; Shah, Amna Z. ; Waseem, Naushin H....
Human Molecular Genetics.  21 (2012)  18 - p. 4126-4137 , 2012
Link: https://doi.org/10.1093/..
 
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13

Prevalence and novelty of PRPF31 mutations in French autoso..:

Audo, Isabelle ; Bujakowska, Kinga ; Mohand-Saïd, Saddek...
BMC Medical Genetics.  11 (2010)  1 - p. , 2010
Link: https://doi.org/10.1186/..
 
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14

Loss of lysophosphatidylcholine acyltransferase 1 leads to ..:

Friedman, James S. ; Chang, Bo ; Krauth, Daniel S....
Proceedings of the National Academy of Sciences.  107 (2010)  35 - p. 15523-15528 , 2010
Link: https://doi.org/10.1073/..
 
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15

Loss of lysophosphatidylcholine acyltransferase 1 leads to ..:

Friedman, James S. ; Chang, Bo ; Krauth, Daniel S....
Proceedings of the National Academy of Sciences of the United States of America.  107 (2010)  35 - p. 15523-15528 , 2010
Link: https://www.jstor.org/st..
 
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