Results 51 to 60 of about 1,142,799 (204)

The Endothelial CXCR Family in Vascular Health and Disease

iNew Medicine, EarlyView.
ABSTRACT Endothelial cells (ECs) form the dynamic interface between blood and tissue, serving as key regulators of vascular homeostasis, inflammation, and repair. Among the molecular systems governing endothelial behavior, the C‐X‐C motif chemokine receptor (CXCR) family—originally characterized in immunology for its roles in leukocyte trafficking and ...
Zhiming Wu, Yandi Wu, Suowen Xu, Yu Huang, Li Wang   +4 more
wiley   +1 more source

ASSOCIATION OF NF-1 AND MOYAMOYA SYNDROME : CASE REPORT

Hematology, Transfusion and Cell Therapy, 2022
Introduction: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder. NF-1 vasculopathy is a significant complication of the disease. It affects both arterial and venous blood vessels of all sizes.
Serap Karaman, Şifa Şahin, Edibe Pembegül Yıldız, Hikmet Gülşah Tanyıldız, Mehmet Barburoğlu, Tutku Turgut, Yasin Yılmaz, Zeynep Karakaş, Deniz Tuğcu, Ayşegül Ünüvar   +9 more
doaj   +1 more source

Calibration‐Free Estimation of Cerebrovascular Reactivity From Resting‐State BOLD fMRI Using Reconstructed Respiratory Fluctuations

Magnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose Cerebrovascular reactivity (CVR) provides an important index of vascular health and is conventionally quantified using a hypercapnic gas or breath‐hold challenge in conjunction with blood‐oxygen‐level‐dependent functional magnetic resonance imaging (BOLD‐fMRI).
Abdoljalil Addeh, Ethan Church, Muhammad Mahajna, Karen Ardila, Pattarawut Charatpangoon, Alexander D. Cohen, Yang Wang, Rebecca J. Williams, G. Bruce Pike, M. Ethan MacDonald   +9 more
wiley   +1 more source

Moyamoya Syndrome Associated with Henoch-Schönlein Purpura [PDF]

, 2016
How to Cite This Article: Shiari R, Tabatabaei Nodushan SMH, Mohebbi MM, Karimzadeh P, Javadzadeh M. Moyamoya Syndrome Associated with Henoch-Schönlein Purpura. Iran J Child Neurol. Autumn 2016; 10(4):71-74.AbstractSome reports have shown the association
SHIARI, Reza, KARIMZADEH, Parvaneh, MOHEBBI, Mohamad Mahdi, TABATABAEI NODUSHAN, Seyed Mohamad Hossein, JAVADZADEH, Mohsen   +4 more
core   +1 more source

Laparoscopic Splenectomy in a Child with Moyamoya Syndrome, Hereditary Spherocytosis, and Interstitial Lung Disease: A Mere Coincidence or Partnership Based on Genetic Similarities

Case Reports in Anesthesiology, 2011
A case of moyamoya syndrome and spherocytosis with concurrent interstitial lung disease who underwent laparoscopic splenectomy is being reported. A theory regarding their coexistence is being forwarded together with their anesthetic management. According
Kasra Karvandian, Zahid Hussain Khan, Jayran Zebardast, Sayed Rohollah Miri   +3 more
doaj   +1 more source

Characterization of inpatient moyamoya in the United States: 1988-2004

Frontiers in Neurology, 2011
Background and Purpose: Moyamoya disease has been classically described by the Asian experience, yet clinical aspects of moyamoya phenomena in the United States remain vastly undefined.
Darrin J Lee, David S Liebeskind
doaj   +1 more source

Primary Cutaneous Gamma‐Delta T‐Cell Lymphoma Complicating Long‐Standing Immunosuppressed Dermatomyositis

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Primary cutaneous gamma‐delta T‐cell lymphoma (PCGD‐TCL) is a rare cytotoxic lymphoma with key oncogenic drivers in the JAK/STAT pathway. Also primarily involving the subcutaneous adipose tissue, subcutaneous panniculitis‐like T‐cell lymphoma (SPTCL) is more frequently encountered in scenarios of autoimmune disorders.
Bennett Christie‐Nguyen, Youn H. Kim, David F. Fiorentino, Danielle Tartar, Ryanne Brown, Robert A. Novoa, Kerri E. Rieger   +6 more
wiley   +1 more source

Moyamoya associated with Turner syndrome in a patient with type 2 spinocerebellar ataxia—Occam’s razor or Hickam’s dictum: a case report

BMC Neurology, 2022
Background Turner syndrome (TS) is a rare condition associated with a completely or partially missing X chromosome that affects 1 in 2500 girls. TS increases the risk of autoimmune diseases, including Graves’ disease (GD).
Paulo Ribeiro Nóbrega, Francisco Bruno Santana da Costa, Pedro Gustavo Barros Rodrigues, Thais de Maria Frota Vasconcelos, Danyela Martins Bezerra Soares, Jéssica Silveira Araújo, Daniel Aguiar Dias, Manoel Alves Sobreira-Neto, Anderson Rodrigues Brandão de Paiva, Pedro Braga-Neto, Fernando Kok, Eveline Gadelha Pereira Fontenele   +11 more
doaj   +1 more source

Inborn errors of immunity in children with neuroinflammation

Developmental Medicine &Child Neurology, EarlyView.
Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu, Dilan Dissanayake, Jessie Cunningham, Helen Branson, Ori Scott, E Ann Yeh   +5 more
wiley   +1 more source

Diseases associated with moyamoya disease or moyamoya syndrome as well as extracerebral vascular manifestations

, 2020
Hintergrund: Bei der Moyamoya-Erkrankung handelt es sich um eine neurovaskuläre Erkrankung, die mit progredienten Stenosierungen der intrakraniellen Anteile der Arteria carotis interna und ihrer Äste und der Bildung eines Kollateralnetzes einhergeht ...
Anselm, Mareike
core   +1 more source