Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous system

Precise Spatiotemporal Control of Nodal Na+ Channel Clustering by Bone Morphogenetic Protein-1/Tolloid-like Proteinases

(2020) Yael Eshed-Eisenbach et al.   NEURON

Mechanisms of node of Ranvier assembly

(2020) Matthew N. Rasband et al.   NATURE REVIEWS NEUROSCIENCE

Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency

(2019) Ismail Solmaz et al.   NEUROPEDIATRICS

CD59 deficiency presenting as polyneuropathy and Moyamoya syndrome with endothelial abnormalities of small brain vessels

(2018) Christian Klemann et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Establishing the role ofPLVAPin protein-losing enteropathy: a homozygous missense variant leads to an attenuated phenotype

(2018) Alina Kurolap et al.   JOURNAL OF MEDICAL GENETICS

Prothrombotic mechanisms in patients with congenital p.Cys89Tyr mutation in CD59

(2018) Adi Tabib et al.   THROMBOSIS RESEARCH

The Axon-Myelin Unit in Development and Degenerative Disease

(2018) Ruth M. Stassart et al.   Frontiers in Neuroscience

Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutations

(2017) Adi Tabib et al.   MOLECULAR IMMUNOLOGY

Neonatal-Onset Recurrent Guillain–Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency

(2017) Didem Ardicli et al.   NEUROPEDIATRICS

Loss of CD55 in Eculizumab-Responsive Protein-Losing Enteropathy

(2017) Alina Kurolap et al.   NEW ENGLAND JOURNAL OF MEDICINE

The Complement Regulatory Protein CD46 Deficient Mouse Spontaneously Develops Dry-Type Age-Related Macular Degeneration–Like Phenotype

(2016) Valeriy V. Lyzogubov et al.   AMERICAN JOURNAL OF PATHOLOGY

Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutation

(2016) Dror Mevorach et al.   ANNALS OF NEUROLOGY

Protection of host cells by complement regulators

(2016) Christoph Q. Schmidt et al.   IMMUNOLOGICAL REVIEWS

Devastating recurrent brain ischemic infarctions and retinal disease in pediatric patients with CD59 deficiency

(2015) Bruria Ben-Zeev et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Paroxysmal nocturnal hemoglobinuria (PNH) and primary p.Cys89Tyr mutation in CD59: Differences and similarities

(2015) Dror Mevorach   MOLECULAR IMMUNOLOGY

Early-onset chronic axonal neuropathy, strokes, and hemolysis: Inherited CD59 deficiency

(2015) G. Haliloglu et al.   NEUROLOGY

Complement Regulatory Protein CD46 Protects against Choroidal Neovascularization in Mice

(2014) Valeriy Lyzogubov et al.   AMERICAN JOURNAL OF PATHOLOGY

Targeted Therapy with Eculizumab for Inherited CD59 Deficiency

(2014) Britta Höchsmann et al.   NEW ENGLAND JOURNAL OF MEDICINE

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy

(2012) Y. Nevo et al.   BLOOD

Guillain–Barré Syndrome

(2012) Nobuhiro Yuki et al.   NEW ENGLAND JOURNAL OF MEDICINE

Structures of the rat complement regulator CrrY

(2011) Pietro Roversi et al.   Acta Crystallographica Section F-Structural Biology and Crystallization Communications

Complement: a key system for immune surveillance and homeostasis

(2010) Daniel Ricklin et al.   NATURE IMMUNOLOGY

A Glial Signal Consisting of Gliomedin and NrCAM Clusters Axonal Na+ Channels during the Formation of Nodes of Ranvier

(2010) Konstantin Feinberg et al.   NEURON

The neuropathic potential of anti-GM1 autoantibodies is regulated by the local glycolipid environment in mice

(2009) Kay N. Greenshields et al.   JOURNAL OF CLINICAL INVESTIGATION

A Novel Model to Measure the Regenerative Potential of the Peripheral Nervous System after Experimental Immunological Demyelination

(2009) Aaron M. Kosins et al.   PLASTIC AND RECONSTRUCTIVE SURGERY