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An economically viable ionic liquid for the fractionation of lignocellulosic biomass

Green chemistry : an international journal and green chemistry resource : GC, 2017, Vol.19 (13), p.3078-3102

2017

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Intramuscular fibrous tissue determines muscle echo intensity in amyotrophic lateral sclerosis

Muscle & nerve, 2012-03, Vol.45 (3), p.449-450

2012

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The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

Journal of neurology, 2019-04, Vol.266 (4), p.876-887

2019

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RYR1-related myopathies: a wide spectrum of phenotypes throughout life

European journal of neurology, 2015-07, Vol.22 (7), p.1094-1112

2015

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Ectopic sphenoidal ACTH-secreting adenoma revealed by 11C Methionine PET scan: case report

BMC endocrine disorders, 2023-02, Vol.23 (1), p.1-43, Article 43

2023

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fMRI reveals distinct CNS processing during symptomatic and recovered complex regional pain syndrome in children

Brain (London, England : 1878), 2008-07, Vol.131 (7), p.1854-1879

2008

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Intestinal hypomotility in systemic sclerosis: a histological study into the sequence of events

Clinical rheumatology, 2021-03, Vol.40 (3), p.981-990

2021

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Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Neuromuscular disorders : NMD, 2013-07, Vol.23 (7), p.540-548

2013

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Simulating the fate of Florida Snowy Plovers with sea-level rise: Exploring research and management priorities with a global uncertainty and sensitivity analysis perspective

Ecological modelling, 2012-01, Vol.224 (1), p.33-47

2012

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Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer: An atypical case of Hu-antibody syndrome

Clinical neurology and neurosurgery, 2020-07, Vol.194, p.105849-105849, Article 105849

2020

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Synthesis of Biobased Succinonitrile from Glutamic Acid and Glutamine

ChemSusChem, 2011-06, Vol.4 (6), p.785-791

2011

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Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I

Clinical genetics, 2018-02, Vol.93 (2), p.255-265

2018

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Skeletal Muscle Ultrasound: Correlation Between Fibrous Tissue and Echo Intensity

Ultrasound in medicine & biology, 2009-03, Vol.35 (3), p.443-446

2009

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Ultrasound‐guided approach to nerves (direct vs. tangential) and the incidence of intraneural injection: a cadaveric study

Anaesthesia, 2017-04, Vol.72 (4), p.461-469

2017

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Practical and reproducible estimation of myenteric interstitial cells of Cajal in the bowel for diagnostic purposes

Neurogastroenterology and motility, 2016-08, Vol.28 (8), p.1261-1267

2016

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Two Cases of Post-Traumatic Mucormycosis due to Mucor circinelloides: Salvage Therapy with a Combination of Adjunctive Therapies

Case reports in infectious diseases, 2022, Vol.2022, p.4949426-8

2022

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Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola disease

Acta neurologica Belgica, 2018-12, Vol.118 (4), p.607-615

2018

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A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi–Goutières syndrome

American journal of medical genetics. Part A, 2010-10, Vol.152A (10), p.2612-2617

2010

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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

Brain (London, England : 1878), 2009-07, Vol.132 (7), p.1741-1752

2009

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Meningoencephalitis with Streptococcus equi Subspecies equi Leading to a Dural Arteriovenous Fistula

Case reports in neurological medicine, 2021-04, Vol.2021, p.1-6

2021

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Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: a review of literature and a cross-sectional clinical study in 17 patients

Neuromuscular disorders : NMD, 2012-11, Vol.22 (11), p.944-954

2012

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Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP

Neurology, 2005-12, Vol.65 (12), p.1924

2005

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Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences

Journal of clinical oncology, 2010-06, Vol.28 (18), p.3008-3014

2010

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Development and developmental disorders of the human cerebellum

Journal of neurology, 2003-09, Vol.250 (9), p.1025-1036

2003

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Congenital myopathy caused by a novel missense mutation in the CFL2 gene

Neuromuscular disorders : NMD, 2012-07, Vol.22 (7), p.632-639

2012

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An economically viable ionic liquid for the fractionation of lignocellulosic biomass

Intramuscular fibrous tissue determines muscle echo intensity in amyotrophic lateral sclerosis

The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

RYR1-related myopathies: a wide spectrum of phenotypes throughout life

Ectopic sphenoidal ACTH-secreting adenoma revealed by 11C Methionine PET scan: case report

fMRI reveals distinct CNS processing during symptomatic and recovered complex regional pain syndrome in children

Intestinal hypomotility in systemic sclerosis: a histological study into the sequence of events

Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Simulating the fate of Florida Snowy Plovers with sea-level rise: Exploring research and management priorities with a global uncertainty and sensitivity analysis perspective

Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer: An atypical case of Hu-antibody syndrome

Synthesis of Biobased Succinonitrile from Glutamic Acid and Glutamine

Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I

Skeletal Muscle Ultrasound: Correlation Between Fibrous Tissue and Echo Intensity

Ultrasound‐guided approach to nerves (direct vs. tangential) and the incidence of intraneural injection: a cadaveric study

Practical and reproducible estimation of myenteric interstitial cells of Cajal in the bowel for diagnostic purposes

Two Cases of Post-Traumatic Mucormycosis due to Mucor circinelloides: Salvage Therapy with a Combination of Adjunctive Therapies

Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola disease

A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi–Goutières syndrome

Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

Meningoencephalitis with Streptococcus equi Subspecies equi Leading to a Dural Arteriovenous Fistula

Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: a review of literature and a cross-sectional clinical study in 17 patients

Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP

Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences

Development and developmental disorders of the human cerebellum

Congenital myopathy caused by a novel missense mutation in the CFL2 gene

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