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Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management

Brain & development (Tokyo. 1979), 2017-05, Vol.39 (5), p.369-385

2017

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Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy

Mitochondrion, 2021-09, Vol.60, p.12-20

2021

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Boundary control of a circular curved beam using active disturbance rejection control

International journal of control, 2019-05, Vol.92 (5), p.1137-1154

Tavasoli, Ali

2019

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A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C

European journal of neurology, 2021-09, Vol.28 (9), p.3040-3050

2021

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Robust Adaptive Boundary Control of a Perturbed Hybrid Euler-Bernoulli Beam with Coupled Rigid and Flexible Motion

International journal of control, automation, and systems, 2022-07, p.680-688

Ali Tavasoli

2022

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An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies

Expert review of neurotherapeutics, 2020-01, Vol.20 (1), p.65-84

2020

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Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients

Neuropediatrics, 2019-04, Vol.50 (2), p.130

2019

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Two-time scale control and observer design for trajectory tracking of two cooperating robot manipulators moving a flexible beam

Robotics and autonomous systems, 2009-02, Vol.57 (2), p.212-221

2009

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Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability

Genomics (San Diego, Calif.), 2020-11, Vol.112 (6), p.4072-4077

2020

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Active disturbance rejection boundary control of Timoshenko beam with tip mass

ISA transactions, 2018-09, Vol.80, p.221-231

Tavasoli, Ali

2018

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Robust boundary stabilization of a vibrating rectangular plate using disturbance adaptation

International journal of adaptive control and signal processing, 2016-11, Vol.30 (11), p.1603-1626

Tavasoli, Ali

2016

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Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants

Scientific reports, 2021-02, Vol.11 (1), p.3231-3231, Article 3231

2021

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Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum

Human mutation, 2021-05, Vol.42 (5), p.491-497

2021

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Well-posedness and exponential stability of two-dimensional vibration model of a boundary-controlled curved beam with tip mass

International journal of systems science, 2018-10, Vol.49 (13), p.2847-2860

Tavasoli, Ali

2018

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Optimized coordination of brakes and active steering for a 4WS passenger car

ISA transactions, 2012-09, Vol.51 (5), p.573-583

2012

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Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations

Orphanet journal of rare diseases, 2018-08, Vol.13 (1), p.130-130, Article 130

2018

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Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trial

Stem cell research & therapy, 2021-08, Vol.12 (1), p.1-15, Article 439

2021

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Efficacy and Safety of Cinnarizine in the Prophylaxis of Migraine in Children: A Double-Blind Placebo-Controlled Randomized Trial

Pediatric neurology, 2014-10, Vol.51 (4), p.503-508

2014

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Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review

Brain & development (Tokyo. 1979), 2017-09, Vol.39 (8), p.714-716

2017

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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Orphanet journal of rare diseases, 2023-07, Vol.18 (1), p.177-177, Article 177

2023

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Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report

BMC pediatrics, 2022-07, Vol.22 (1), p.1-412, Article 412

2022

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Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Orphanet journal of rare diseases, 2023-07, Vol.18 (1), p.190-190, Article 190

2023

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Adaptive robust boundary control of shaft vibrations under perturbations with unknown upper bounds

International journal of adaptive control and signal processing, 2015-05, Vol.29 (5), p.537-562

Tavasoli, Ali

2015

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Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy

BMC neurology, 2022-05, Vol.22 (1), p.162-162, Article 162

2022

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RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant

Orphanet journal of rare diseases, 2019-07, Vol.14 (1), p.184-7, Article 184

2019

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Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management

Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy

Boundary control of a circular curved beam using active disturbance rejection control

A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C

Robust Adaptive Boundary Control of a Perturbed Hybrid Euler-Bernoulli Beam with Coupled Rigid and Flexible Motion

An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies

Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients

Two-time scale control and observer design for trajectory tracking of two cooperating robot manipulators moving a flexible beam

Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability

Active disturbance rejection boundary control of Timoshenko beam with tip mass

Robust boundary stabilization of a vibrating rectangular plate using disturbance adaptation

Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants

Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum

Well-posedness and exponential stability of two-dimensional vibration model of a boundary-controlled curved beam with tip mass

Optimized coordination of brakes and active steering for a 4WS passenger car

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations

Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trial

Efficacy and Safety of Cinnarizine in the Prophylaxis of Migraine in Children: A Double-Blind Placebo-Controlled Randomized Trial

Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Adaptive robust boundary control of shaft vibrations under perturbations with unknown upper bounds

Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy

RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant

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