Search details
1.
Neurofilament light protein as a biomarker for spinal muscular atrophy: a review and reference ranges.
Clin Chem Lab Med
; 62(7): 1252-1265, 2024 Jun 25.
Article
in English
| MEDLINE | ID: mdl-38215341
2.
Therapeutic Approaches to Type I Interferonopathies.
Curr Rheumatol Rep
; 20(6): 32, 2018 04 20.
Article
in English
| MEDLINE | ID: mdl-29679241
3.
Familial chilblain lupus due to a gain-of-function mutation in STING.
Ann Rheum Dis
; 76(2): 468-472, 2017 Feb.
Article
in English
| MEDLINE | ID: mdl-27566796
4.
Troponin T is elevated in a relevant proportion of patients with 5q-associated spinal muscular atrophy.
Sci Rep
; 14(1): 6634, 2024 03 19.
Article
in English
| MEDLINE | ID: mdl-38503830
5.
Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1ß.
Hum Mutat
; 34(1): 122-31, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-22833538
6.
Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome.
Neurol Neuroimmunol Neuroinflamm
; 9(6)2022 11.
Article
in English
| MEDLINE | ID: mdl-36229191
7.
Response to: 'JAK inhibition in STING-associated interferonopathy' by Crow et al.
Ann Rheum Dis
; 75(12): e76, 2016 12.
Article
in English
| MEDLINE | ID: mdl-27811148
8.
Thymulin-based gene therapy and pituitary function in animal models of aging.
Neuroimmunomodulation
; 18(5): 350-6, 2011.
Article
in English
| MEDLINE | ID: mdl-21952687
9.
Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children.
Ann Clin Transl Neurol
; 8(10): 2013-2024, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34482646
10.
High association of MOG-IgG antibodies in children with bilateral optic neuritis.
Eur J Paediatr Neurol
; 27: 86-93, 2020 Jul.
Article
in English
| MEDLINE | ID: mdl-32327391
11.
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene.
Eur J Paediatr Neurol
; 22(1): 186-189, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-29221912
12.
Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis.
J Neurol
; 268(6): 2259-2262, 2021 Jun.
Article
in English
| MEDLINE | ID: mdl-33751187
13.
Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation.
Neurol Genet
; 6(1): e384, 2020 Feb.
Article
in English
| MEDLINE | ID: mdl-32042913
14.
Defective removal of ribonucleotides from DNA promotes systemic autoimmunity.
J Clin Invest
; 125(1): 413-24, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25500883
15.
Single-stranded nucleic acids promote SAMHD1 complex formation.
J Mol Med (Berl)
; 91(6): 759-70, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23371319
16.
Management of external small bowel fistulae: challenges and controversies confronting the general surgeon.
Int J Surg
; 9(3): 198-203, 2011.
Article
in English
| MEDLINE | ID: mdl-21111073
17.
Effect of intestinal pressure on fistula closure during vacuum assisted treatment: a computational approach.
Int J Surg
; 9(8): 662-8, 2011.
Article
in English
| MEDLINE | ID: mdl-21945673
Results
1 -
17
de 17
1
Next >
>>