Articles with "five patients" as a keyword



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Anti-phospholipid syndrome associated with schizophrenia description of five patients and review of the literature

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Published in 2017 at "Immunologic Research"

DOI: 10.1007/s12026-017-8895-1

Abstract: Anti-phospholipid syndrome is an autoimmune disorder characterized by anti-phospholipid antibodies, arterial and venous thrombosis, pregnancy morbidity, and various neurological manifestations including psychiatric disorders. Higher incidence of various autoimmune disorders was found in schizophrenia. In addition,… read more here.

Keywords: syndrome associated; associated schizophrenia; five patients; anti phospholipid ... See more keywords
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Recognition of Neonatal Lymphatic Flow Disorder: Fetal MR Findings and Postnatal MR Lymphangiogram Correlation.

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Published in 2018 at "Academic radiology"

DOI: 10.1016/j.acra.2018.02.020

Abstract: RATIONALE AND OBJECTIVES This study aimed to describe prenatal and postnatal imaging features and outcomes of neonates with neonatal lymphatic disorders (NLDs). MATERIALS AND METHODS An institutional review board-approved search of the radiology database for… read more here.

Keywords: neonatal lymphatic; disorder; five patients; radiology ... See more keywords
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A Case Series of Five Patients With Pure or Mixed Gestational Epithelioid Trophoblastic Tumors and a Literature Review on Mixed Tumors

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Published in 2018 at "American Journal of Clinical Pathology"

DOI: 10.1093/ajcp/aqy039

Abstract: Objectives To review the clinicopathologic features of five patients with epithelioid trophoblastic tumor (ETT). Methods Characteristics of patients diagnosed with ETT in 2000 to 2012 were reviewed. Results Among 190 patients with gestational trophoblastic neoplasia… read more here.

Keywords: mixed tumors; five patients; case series; pure ett ... See more keywords
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Missense variants in ALAS2 gene in five patients

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Published in 2019 at "International Journal of Laboratory Hematology"

DOI: 10.1111/ijlh.12902

Abstract: Sideroblastic anemias (SAs) are a heterozygous group of disorders characterized by the presence of ring sideroblasts in the bone marrow. Congenital sideroblastic anemias are syndromic and nonsyndromic and caused by pathogenic variants in genes involved… read more here.

Keywords: variants alas2; missense variants; alas2 gene; five patients ... See more keywords
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Unusual cases of peritonitis: A case series of five patients

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Published in 2022 at "Seminars in Dialysis"

DOI: 10.1111/sdi.13121

Abstract: Introduction: Peritonitis is a complication in patients on peritoneal dialysis that frequently results from touch contamination. Most cases of peritoneal dialysis‐related peritonitis are caused by skin organisms. Herein, we are presenting a series of peritonitis… read more here.

Keywords: peritonitis; patients unusual; five patients; series ... See more keywords
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Proof-of-concept study of electrospun PLGA membrane in the treatment of limbal stem cell deficiency

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Published in 2021 at "BMJ Open Ophthalmology"

DOI: 10.1136/bmjophth-2021-000762

Abstract: Objective The aim of this study was to assess the safety of poly-lactic co-glycolic acid (PLGA) electrospun membranes as carriers for limbal tissue explants for treatment of limbal stem cell deficiency (LSCD). Methods and analysis… read more here.

Keywords: five patients; study; limbal stem; treatment limbal ... See more keywords
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High efficacy of PD-1 inhibitor after initial failure of PD-L1 inhibitor in Relapsed/Refractory classical Hodgkin Lymphoma

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Published in 2022 at "BMC Cancer"

DOI: 10.1186/s12885-021-09028-4

Abstract: Purpose We sought to understand the clinical course and molecular phenotype of patients who showed disease progression after programmed cell death ligand 1 (PD-L1) inhibitor treatment but subsequently responded to PD-1 inhibitor treatment. We also… read more here.

Keywords: five patients; relapsed refractory; inhibitor; hodgkin lymphoma ... See more keywords
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Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China–expanding the atypical phenotypes

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Published in 2022 at "Frontiers in Immunology"

DOI: 10.3389/fimmu.2022.972746

Abstract: Background Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder of the immune regulatory system caused by forkhead box P3 (FOXP3) mutations. Abnormal numbers or functions of regulatory T (Treg) cells account for… read more here.

Keywords: syndrome china; five patients; immune dysregulation; dysregulation polyendocrinopathy ... See more keywords
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Analysis of Clinical and Genetic Characterization of Three Ataxia–Telangiectasia Pedigrees With Novel ATM Gene Mutations

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Published in 2022 at "Frontiers in Pediatrics"

DOI: 10.3389/fped.2022.877826

Abstract: Objective The clinical manifestations of ataxia–telangiectasia (AT) are very complex and are easily misdiagnosed and missed. The purpose of this study was to explore the clinical characteristics and genetic features of five pediatric patients with… read more here.

Keywords: ataxia telangiectasia; telangiectasia; five patients; atm gene ... See more keywords
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Abatacept Rescue Therapy in Kidney Transplant Recipients: A Case Series of Five Patients

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Published in 2022 at "Transplant International"

DOI: 10.3389/ti.2022.10681

Abstract: Dear Editors, Abatacept, a cytotoxic T-lymphocyte-associated antigen 4 immunoglobulin (CTLA4-Ig), is a subcutaneously administered immunosuppressive drug that selectively inhibits T-cell activation by blocking the CD28-CD80/86 costimulatory pathway. Abatacept is widely used in rheumatology, especially in… read more here.

Keywords: five patients; abatacept rescue; therapy; rescue therapy ... See more keywords