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Reply to comment on ‘Accelerating a car from rest: friction, power and forces’

Physics education, 2024-05, Vol.59 (3), p.38002

2024

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Accelerating a car from rest: friction, power and forces

Physics education, 2023-09, Vol.58 (5), p.55005

2023

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Estimated intracranial volume from FreeSurfer is biased by total brain volume

European radiology experimental, 2018-09, Vol.2 (1), p.1-6, Article 24

2018

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A Longitudinal Study of Medial Temporal Lobe Volumes in Graves Disease

The journal of clinical endocrinology and metabolism, 2022-03, Vol.107 (4), p.1040-1052

2022

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Delineation of two intracranial areas and the perpendicular intracranial width is sufficient for intracranial volume estimation

Insights into imaging, 2018-02, Vol.9 (1), p.25-34

2018

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White Matter Lesion Assessment in Patients with Cognitive Impairment and Healthy Controls: Reliability Comparisons between Visual Rating, a Manual, and an Automatic Volumetrical MRI Method-The Gothenburg MCI Study

Journal of Aging Research, 2013, Vol.2013 (2013), p.24-33

2013

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Structural brain changes in hyperthyroid Graves’ disease: protocol for an ongoing longitudinal, case-controlled study in Göteborg, Sweden—the CogThy project

BMJ open, 2019-11, Vol.9 (11), p.e031168-e031168

2019

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High white matter lesion load is associated with hippocampal atrophy in mild cognitive impairment

Dementia and geriatric cognitive disorders, 2011-01, Vol.31 (2), p.132-138

2011

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Valid and efficient manual estimates of intracranial volume from magnetic resonance images

BMC medical imaging, 2015-02, Vol.15 (1), p.5-5, Article 5

2015

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NIPT – implentation, counselling and ethical issues

Läkartidningen, 2017-05, Vol.114

2017

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Replik från SFOG: - Ultraljud och NIPT till alla är önskvärt, men inte realistiskt: Replik från SFOG: - Ultraljud och NIPT till alla är önskvärt, men inte realistiskt

Läkartidningen, 2017-06, Vol.114

2017

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Inherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: Inter- and intra-individual variation and correlation to the phenotype

American journal of medical genetics. Part A, 2012-05, Vol.158A (5), p.1111-1117

2012

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Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities

Pediatric blood & cancer, 2009-12, Vol.53 (6), p.1143-1146

2009

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Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome

Human molecular genetics, 1995-04, Vol.4 (4), p.615-621

1995

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Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome

European journal of human genetics : EJHG, 1995, Vol.3 (4), p.219-227

1995

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Rapid detection of a mutation hot-spot in the human androgen receptor

Clinical genetics, 1996-10, Vol.50 (4), p.202-205

1996

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Beyond 3G radio access network reference architecture

2004 IEEE 59th Vehicular Technology Conference. VTC 2004-Spring (IEEE Cat. No.04CH37514), 2004, Vol.4, p.2047-2051 Vol.4

2004

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Strong founder effect for the fragile X syndrome in Sweden

European journal of human genetics : EJHG, 1994, Vol.2 (2), p.103-109

1994

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Linkage mapping of a severe X-linked mental retardation syndrome

American journal of human genetics, 1993-06, Vol.52 (6), p.1046-1052

1993

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METHYLATION AND MUTATION PATTERNS IN THE FRAGILE X SYNDROME

Pediatric research, 1992-11, Vol.32 (5), p.621-621

1992

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New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death

American journal of medical genetics, 1993-03, Vol.45 (5), p.654-658

1993

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Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries

American journal of medical genetics, 1992-04, Vol.43 (1-2), p.353-354

1992

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Methylation and mutation patterns in the fragile X syndrome

American journal of medical genetics, 1992-04, Vol.43 (1-2), p.268-278

1992

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Infantile autism-fragile X: Molecular findings support genetic heterogeneity

American journal of medical genetics, 1992-12, Vol.44 (6), p.830-833

1992

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Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.319-321

1991

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Reply to comment on ‘Accelerating a car from rest: friction, power and forces’

Accelerating a car from rest: friction, power and forces

Estimated intracranial volume from FreeSurfer is biased by total brain volume

A Longitudinal Study of Medial Temporal Lobe Volumes in Graves Disease

Delineation of two intracranial areas and the perpendicular intracranial width is sufficient for intracranial volume estimation

White Matter Lesion Assessment in Patients with Cognitive Impairment and Healthy Controls: Reliability Comparisons between Visual Rating, a Manual, and an Automatic Volumetrical MRI Method-The Gothenburg MCI Study

Structural brain changes in hyperthyroid Graves’ disease: protocol for an ongoing longitudinal, case-controlled study in Göteborg, Sweden—the CogThy project

High white matter lesion load is associated with hippocampal atrophy in mild cognitive impairment

Valid and efficient manual estimates of intracranial volume from magnetic resonance images

NIPT – implentation, counselling and ethical issues

Replik från SFOG: - Ultraljud och NIPT till alla är önskvärt, men inte realistiskt: Replik från SFOG: - Ultraljud och NIPT till alla är önskvärt, men inte realistiskt

Inherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: Inter- and intra-individual variation and correlation to the phenotype

Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities

Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome

Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome

Rapid detection of a mutation hot-spot in the human androgen receptor

Beyond 3G radio access network reference architecture

Strong founder effect for the fragile X syndrome in Sweden

Linkage mapping of a severe X-linked mental retardation syndrome

METHYLATION AND MUTATION PATTERNS IN THE FRAGILE X SYNDROME

New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death

Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries

Methylation and mutation patterns in the fragile X syndrome

Infantile autism-fragile X: Molecular findings support genetic heterogeneity

Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304

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