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Pediatric Rheumatology Online Journal
|
January 4, 2024
A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
Sophia Weidler, Sarah Koss, Christine Wolf, et al.
Nature Immunology
|
September 28, 2010
The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1
Nan Yan, Ashton D Regalado-Magdos, Bart Stiggelbout, et al.
Journal of Child Neurology
|
March 5, 2009
Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 gene
Georgia Ramantani, Pascal Niggemann, Gabriele Hahn, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic Ribonucleotides
Barbara Kind, Christine Wolf, Kerstin Engel, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))
|
April 16, 2021
[How Often is Rare Really Rare? A Survey on the Frequency of Rare Diseases at a University Hospital]
Tanita Kretschmer, Adrian Danker, Olaf Müller, et al.
Stem Cell Research
|
August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutations
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Stem Cell Research
|
September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutations
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Frontiers in Immunology
|
October 9, 2023
Case Report: Response of cutaneous lupus lesions in SLE to interferon receptor blockade parallels reduction of interferon score in blood
Claudia Günther, Christine Wolf, Louisa Fennen, et al.
Pediatric Rheumatology Online Journal
|
September 19, 2023
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositis
Timmy Strauss, Claudia Günther, Anja Schnabel, et al.
Pediatric Rheumatology Online Journal
|
April 12, 2022
Precision treatment of Singleton Merten syndrome with ruxolitinib: a case report
Philip Broser, Ursula von Mengershausen, Katrin Heldt, et al.
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of 9
Search research articles
Search
Showing results (11-20 of 86) with videos related to
Sort By:
Page
of 9
Pediatric Rheumatology Online Journal
|
January 4, 2024
A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
Sophia Weidler, Sarah Koss, Christine Wolf, et al.
Nature Immunology
|
September 28, 2010
The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1
Nan Yan, Ashton D Regalado-Magdos, Bart Stiggelbout, et al.
Journal of Child Neurology
|
March 5, 2009
Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 gene
Georgia Ramantani, Pascal Niggemann, Gabriele Hahn, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic Ribonucleotides
Barbara Kind, Christine Wolf, Kerstin Engel, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))
|
April 16, 2021
[How Often is Rare Really Rare? A Survey on the Frequency of Rare Diseases at a University Hospital]
Tanita Kretschmer, Adrian Danker, Olaf Müller, et al.
Stem Cell Research
|
August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutations
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Stem Cell Research
|
September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutations
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Frontiers in Immunology
|
October 9, 2023
Case Report: Response of cutaneous lupus lesions in SLE to interferon receptor blockade parallels reduction of interferon score in blood
Claudia Günther, Christine Wolf, Louisa Fennen, et al.
Pediatric Rheumatology Online Journal
|
September 19, 2023
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositis
Timmy Strauss, Claudia Günther, Anja Schnabel, et al.
Pediatric Rheumatology Online Journal
|
April 12, 2022
Precision treatment of Singleton Merten syndrome with ruxolitinib: a case report
Philip Broser, Ursula von Mengershausen, Katrin Heldt, et al.
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of 9