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A nonsense mutation in CEP55 defines a new locus for a Meckel‐like syndrome, an autosomal recessive lethal fetal ciliopathy

Clinical genetics, 2017-11, Vol.92 (5), p.510-516

2017

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Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies

Journal of medical genetics, 2006-04, Vol.43 (4), p.e14-e14

2006

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Diagnosis of placental mesenchymal dysplasia with magnetic resonance imaging

Ultrasound in obstetrics & gynecology, 2017-03, Vol.49 (3), p.410-412

2017

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4D-PET/CT with [11 C]-PK11195 and [11 C]- d -deprenyl Does not Identify the Chronic Inflammation in Asymptomatic Abdominal Aortic Aneurysms

European journal of vascular and endovascular surgery, 2013-04, Vol.45 (4), p.351-356

2013

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Attachment and Mental and Physical Health: Self-Compassion and Mattering as Mediators

Journal of counseling psychology, 2011-04, Vol.58 (2), p.272-278

2011

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FDG-PET on Irradiated Brain Tumor: Ten Years' Summary

Acta radiologica (1987), 2006-02, Vol.47 (1), p.85-90

2006

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Oncogenic PI3K and its role in cancer

Current opinion in oncology, 2006-01, Vol.18 (1), p.77-82

2006

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A wavelet-based expert system for digital subscriber line topology identification

International journal of communication systems, 2016-01, Vol.29 (1), p.47-63

2016

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“Atypical femoral fractures” during bisphosphonate exposure in adult hypophosphatasia

Journal of bone and mineral research, 2012-05, Vol.27 (5), p.987-994

2012

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Effects of 21 days of bed rest, with or without artificial gravity, on nutritional status of humans

Journal of applied physiology (1985), 2009-07, Vol.107 (1), p.54-62

2009

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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

American journal of human genetics, 2001-03, Vol.68 (3), p.590-597

2001

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Expression of cyclin-dependent kinase 6, but not cyclin-dependent kinase 4, alters morphology of cultured mouse astrocytes

Molecular cancer research, 2003-07, Vol.1 (9), p.654-664

2003

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Lymphocytic hypophysitis: report of two biopsy-proven cases and one suspected case with pituitary autoantibodies

Journal of endocrinological investigation, 2007-02, Vol.30 (2), p.153-162

2007

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Urge to scratch represented in the human cerebral cortex during itch

Journal of neurophysiology, 1994-12, Vol.72 (6), p.3004-3008

1994

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036 A Trial of Low-Intensity Shockwave Therapy for Penile Rehabilitation After Radical Prostatectomy

Journal of sexual medicine, 2020-01, Vol.17 (1), p.S19-S20

2020

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Transposon-based interferon gamma gene transfer overcomes limitations of episomal plasmid for immunogene therapy of glioblastoma

Cancer gene therapy, 2007-06, Vol.14 (6), p.550-560

2007

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Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review)

Journal of bone and mineral research, 2011-10, Vol.26 (10), p.2389-2398

2011

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Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy

Journal of bone and mineral research, 2013-02, Vol.28 (2), p.419-430

2013

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Postmortem magnetic resonance imaging vs autopsy of second trimester fetuses terminated due to anomalies

Acta obstetricia et gynecologica Scandinavica, 2019-07, Vol.98 (7), p.865-876

2019

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Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis

American journal of medical genetics. Part A, 2022-06, Vol.188 (6), p.1676-1687

2022

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PRE-SERVICE TEACHERS’ EXPERIENCES OF THE TRANSITION FROM ANALOGUE TO DIGITAL LEARNING DURING THE COVID-19 PANDEMIC

PROBLEMS OF EDUCATION IN THE 21ST CENTURY, 2022-01, Vol.80 (2), p.273-288

2022

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Training Undergraduate Students to Use Interpretation

The Counseling psychologist, 2014-08, Vol.42 (6), p.778-799

2014

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Geomorphological surfaces of different age and origin in granite landscapes: an evaluation of the Schmidt hammer test

Earth surface processes and landforms, 2004-04, Vol.29 (4), p.495-509

Ericson, Kerstin

2004

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Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T > C, p.M226T; c.1112C > T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene

Bone (New York, N.Y.), 2007-06, Vol.40 (6), p.1655-1661

2007

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Training Undergraduate Students to Use Challenges

The Counseling psychologist, 2014-08, Vol.42 (6), p.758-777

2014

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A nonsense mutation in CEP55 defines a new locus for a Meckel‐like syndrome, an autosomal recessive lethal fetal ciliopathy

Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies

Diagnosis of placental mesenchymal dysplasia with magnetic resonance imaging

4D-PET/CT with [11 C]-PK11195 and [11 C]- d -deprenyl Does not Identify the Chronic Inflammation in Asymptomatic Abdominal Aortic Aneurysms

Attachment and Mental and Physical Health: Self-Compassion and Mattering as Mediators

FDG-PET on Irradiated Brain Tumor: Ten Years' Summary

Oncogenic PI3K and its role in cancer

A wavelet-based expert system for digital subscriber line topology identification

“Atypical femoral fractures” during bisphosphonate exposure in adult hypophosphatasia

Effects of 21 days of bed rest, with or without artificial gravity, on nutritional status of humans

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

Expression of cyclin-dependent kinase 6, but not cyclin-dependent kinase 4, alters morphology of cultured mouse astrocytes

Lymphocytic hypophysitis: report of two biopsy-proven cases and one suspected case with pituitary autoantibodies

Urge to scratch represented in the human cerebral cortex during itch

036 A Trial of Low-Intensity Shockwave Therapy for Penile Rehabilitation After Radical Prostatectomy

Transposon-based interferon gamma gene transfer overcomes limitations of episomal plasmid for immunogene therapy of glioblastoma

Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review)

Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy

Postmortem magnetic resonance imaging vs autopsy of second trimester fetuses terminated due to anomalies

Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis

PRE-SERVICE TEACHERS’ EXPERIENCES OF THE TRANSITION FROM ANALOGUE TO DIGITAL LEARNING DURING THE COVID-19 PANDEMIC

Training Undergraduate Students to Use Interpretation

Geomorphological surfaces of different age and origin in granite landscapes: an evaluation of the Schmidt hammer test

Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T > C, p.M226T; c.1112C > T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene

Training Undergraduate Students to Use Challenges

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