I. Nygren

发表

Initial Experience of the Levodopa–Entacapone–Carbidopa Intestinal Gel in Clinical Practice

D. Nyholm, E. Widman, Mezin Öthman, 2021, Journal of personalized medicine.

High resting level and weak response of baroreflex‐governed sympathetic outflow in amyotrophic lateral sclerosis

J. Fagius, I. Nygren, 2011, Muscle & nerve.

Death in hospital following ICU discharge: insights from the LUNG SAFE study

Karen E. Williams, Russell R. Miller, Samuel M. Brown, 2020, Critical Care.

Quality of life among relatives of patients with amyotrophic lateral sclerosis: A prospective and longitudinal study

K. Nordin, B. Larsson, I. Nygren, 2021, Palliative and Supportive Care.

Increased serum and cerebrospinal fluid FGF-2 levels in amyotrophic lateral sclerosis

K. Blennow, A. Larsson, A. Johansson, 2003, Neuroreport.

Physical fitness, but not muscle strength, is a risk factor for death in amyotrophic lateral sclerosis at an early age

Ingrid Lönnstedt, H. Askmark, I. Nygren, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Hyperoxemia and excess oxygen use in early acute respiratory distress syndrome: insights from the LUNG SAFE study

Karen E. Williams, Russell R. Miller, Samuel M. Brown, 2020, Critical Care.

Maintained regulation of polyamines in spinal cord from patients with amyotrophic lateral sclerosis

H. Askmark, I. Nygren, C. Gomes-Trolin, 2004, Journal of the Neurological Sciences.

Increased expression of glial cell line-derived neurotrophic factor mRNA in muscle biopsies from patients with amyotrophic lateral sclerosis

S. Aquilonius, H. Askmark, I. Nygren, 1999, Journal of the Neurological Sciences.

Self-reported quality of life in amyotrophic lateral sclerosis.

H. Askmark, I. Nygren, 2006, Journal of palliative medicine.

The ALS/MND prevalence in Sweden estimated by riluzole sales statistics

H. Askmark, I. Nygren, P. Mattsson, 2005, Acta neurologica Scandinavica.

Death in hospital following ICU discharge: insights from the LUNG SAFE study

Karen E. Williams, John C. Adams, Barrett T. Kitch, 2020, Critical Care.

Vitamin D deficiency in patients with myasthenia gravis and improvement of fatigue after supplementation of vitamin D3: a pilot study

A. Punga, H. Askmark, I. Nygren, 2012, European journal of neurology.

Recurrence of Susac Syndrome following 23 Years of Remission

R. Raininko, H. Larsen, I. Nygren, 2014, Case Reports in Neurology.

Measurement of sCD27 in the cerebrospinal fluid identifies patients with neuroinflammatory disease

K. Kultima, A. Larsson, M. Ingelsson, 2019, Journal of Neuroimmunology.

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients

Berg, S. Newhouse, A. Al-Chalabi, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Increased Red Blood Cell Polyamines in ALS and Parkinson's Disease

S. Aquilonius, H. Askmark, I. Nygren, 2002, Experimental Neurology.

Validation and utility of ARDS subphenotypes identified by machine-learning models using clinical data: an observational, multicohort, retrospective analysis

Sarah L. Gillis, Karen E. Williams, John C. Adams, 2022, The Lancet Respiratory Medicine.

Efficacy and Safety of Rituximab for New-Onset Generalized Myasthenia Gravis

F. Piehl, A. Punga, A. Budzianowska, 2022, JAMA neurology.

Monozygous twins with neuromuscular transmission defects at opposite sides of the motor endplate

E. Stålberg, H. Askmark, I. Nygren, 2009, Acta neurologica Scandinavica.

Epidemiology and patterns of tracheostomy practice in patients with acute respiratory distress syndrome in ICUs across 50 countries

Karen E. Williams, John C. Adams, Barrett T. Kitch, 2018, Critical Care.

Vitamin D deficiency in patients with primary immune-mediated peripheral neuropathies

A. Punga, H. Askmark, K. Elf, 2014, Journal of the Neurological Sciences.

A prospective study of quality of life in amyotrophic lateral sclerosis patients

K. Nordin, I. Nygren, A. Ozanne, 2017, Acta neurologica Scandinavica.

Strong potential for baroreflex-governed sympathetic outflow revealed during nausea

J. Fagius, I. Nygren, 2010, Clinical Autonomic Research.

Alterations in muscle proteome of patients diagnosed with amyotrophic lateral sclerosis.

J. Bergquist, L. Larsson, H. Askmark, 2014, Journal of proteomics.

Geoeconomic variations in epidemiology, ventilation management, and outcomes in invasively ventilated intensive care unit patients without acute respiratory distress syndrome: a pooled analysis of four observational studies

Karen E. Williams, Raquel Siqueira Nóbrega, Christopher G. Smalley, 2021, The Lancet. Global health.

July 2017 ENCALS statement on edaravone

A. Al-Chalabi, P. Andersen, A. Chiò, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

VEGF is increased in serum but not in spinal cord from patients with amyotrophic lateral sclerosis

A. Larsson, A. Johansson, H. Askmark, 2002, Neuroreport.

Mechanical ventilation in patients with cardiogenic pulmonary edema: a sub-analysis of the LUNG SAFE study

Karen E. Williams, John C. Adams, Barrett T. Kitch, 2022, Journal of Intensive Care.

Pain, disease severity and associations with individual quality of life in patients with motor neuron diseases

D. Nyholm, B. Larsson, I. Nygren, 2021, BMC Palliative Care.

Relatives of patients with amyotrophic lateral sclerosis: Their experience of care and support

K. Nordin, B. Larsson, I. Nygren, 2015, Palliative and Supportive Care.

Coping with amyotrophic lateral sclerosis; from diagnosis and during disease progression

K. Nordin, B. Larsson, I. Nygren, 2016, Journal of the Neurological Sciences.

Identifying associations between diabetes and acute respiratory distress syndrome in patients with acute hypoxemic respiratory failure: an analysis of the LUNG SAFE database

Karen E. Williams, John C. Adams, Barrett T. Kitch, 2018, Critical Care.

Coping strategies among patients with newly diagnosed amyotrophic lateral sclerosis.

K. Nordin, H. Askmark, I. Nygren, 2014, Journal of clinical nursing.

Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

C. Lewis, J. Powell, A. Al-Chalabi, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

High resting level and weak response of baroreflex‐governed sympathetic outflow in amyotrophic lateral sclerosis

J. Fagius, I. Nygren, 2011, Muscle & nerve.