Mai K. ElMallah

United States

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Articles (18)

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2025

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (5)

RAM PURANAM

Asst Prof Medical Research

Duke University

UNITED STATES

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Purushothama Rao Tata

Duke University

UNITED STATES

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Jane E. Gross

UNITED STATES

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Elisabeth Tracy

UNITED STATES

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Moshe Prero

UNITED STATES

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Mai K. ElMallah

Research Interests

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Articles (18)

Therapeutic acute intermittent hypoxia modestly improves breathing in Pompe disease

Characteristics of non-sleep related apneas in children with alternating hemiplegia of childhood

ATS Core Curriculum 2022. Pediatric Pulmonary Medicine: Updates in pediatric neuromuscular disease

GAA deficiency disrupts distal airway cells in Pompe disease

Pulmonary manifestations of STAC3 disorder: A case series

Congenital lobar emphysema in monozygotic twins.

Monitoring and Management of Respiratory Function in Pompe Disease: Current Perspectives.

X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease.

Breathing in Duchenne muscular dystrophy: translation to therapy

Neuro-respiratory pathology in spinocerebellar ataxia.

Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing.

Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7

Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3<sup>Mashl/+</sup>, Mouse Model of Alternating Hemiplegia of Childhood

Corrigendum to “Respiratory pathology in the optn<sup>-/-</sup> mouse model of amyotrophic lateral sclerosis” [Respir. Physiol. Neurobiol. 282 (2020) 103525] (Respiratory Physiology & Neurobiology (2020) 282, (S156990482030183X), (10.1016/j.resp.2020.103525))

Genetic deletion of the Tas2r143/Tas2r135/Tas2r126 cluster reveals that TAS2Rs may not mediate bitter tastant-induced bronchodilation

Glycogen Accumulation in Smooth Muscle of A Pompe Disease Mouse Model

The Respiratory Phenotype of Pompe Disease Mouse Models

Comparisons of Infant and Adult Mice Reveal Age Effects for Liver Depot Gene Therapy in Pompe Disease

Collaborators (5)

RAM PURANAM

Purushothama Rao Tata

Jane E. Gross

Elisabeth Tracy

Moshe Prero

Make your next move.

Mai K. ElMallah

Research Interests

Explore related searches

Contact this professor

Articles (18)

Therapeutic acute intermittent hypoxia modestly improves breathing in Pompe disease

Characteristics of non-sleep related apneas in children with alternating hemiplegia of childhood

ATS Core Curriculum 2022. Pediatric Pulmonary Medicine: Updates in pediatric neuromuscular disease

GAA deficiency disrupts distal airway cells in Pompe disease

Pulmonary manifestations of STAC3 disorder: A case series

Congenital lobar emphysema in monozygotic twins.

Monitoring and Management of Respiratory Function in Pompe Disease: Current Perspectives.

X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease.

Breathing in Duchenne muscular dystrophy: translation to therapy

Neuro-respiratory pathology in spinocerebellar ataxia.

Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing.

Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7

Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3<sup>Mashl/+</sup>, Mouse Model of Alternating Hemiplegia of Childhood

Corrigendum to “Respiratory pathology in the optn<sup>-/-</sup> mouse model of amyotrophic lateral sclerosis” [Respir. Physiol. Neurobiol. 282 (2020) 103525] (Respiratory Physiology &amp; Neurobiology (2020) 282, (S156990482030183X), (10.1016/j.resp.2020.103525))

Genetic deletion of the Tas2r143/Tas2r135/Tas2r126 cluster reveals that TAS2Rs may not mediate bitter tastant-induced bronchodilation

Glycogen Accumulation in Smooth Muscle of A Pompe Disease Mouse Model

The Respiratory Phenotype of Pompe Disease Mouse Models

Comparisons of Infant and Adult Mice Reveal Age Effects for Liver Depot Gene Therapy in Pompe Disease

Collaborators (5)

RAM PURANAM

Purushothama Rao Tata

Jane E. Gross

Elisabeth Tracy

Moshe Prero

Make your next move.

Corrigendum to “Respiratory pathology in the optn<sup>-/-</sup> mouse model of amyotrophic lateral sclerosis” [Respir. Physiol. Neurobiol. 282 (2020) 103525] (Respiratory Physiology & Neurobiology (2020) 282, (S156990482030183X), (10.1016/j.resp.2020.103525))