Results 321 to 330 of about 1,034,220 (415)

Mixed Autoimmune Hemolytic Anemia: A Systematic Review of Epidemiology, Clinical Characteristics, Therapies, and Outcomes

open access: yesAmerican Journal of Hematology, EarlyView.
Mixed autoimmune hemolytic anemia (AIHA) is a rare condition characterized by the presence of both warm and cold autoantibodies, often leading to severe, treatment‐resistant hemolysis. In this systematic review of 81 patients across 35 studies, the median age was 45 years with a notable female predominance.
Jeremy W. Jacobs   +12 more
wiley   +1 more source

Comorbid Clinical Conditions in Chronic Fatigue. A Co-Twin Control Study

open access: green, 2001
Leslie A. Aaron   +6 more
openalex   +2 more sources

A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu   +10 more
wiley   +1 more source

Prognostic value of troponin T in hemodialysis patients is independent of comorbidity

open access: bronze, 2001
Patrick Deegan   +4 more
openalex   +1 more source

Sex and depression in the National Comorbidity Survey. I: Lifetime prevalence, chronicity and recurrence.

open access: yesJournal of Affective Disorders, 1993
R. Kessler   +4 more
semanticscholar   +1 more source

Type 1 Diabetes/Hidradenitis Suppurativa Comorbidity-A Population-Based Study. [PDF]

open access: yesJ Clin Med
Sherman S   +8 more
europepmc   +1 more source

Comorbidity among patients with colon cancer in New Zealand [PDF]

open access: yes, 2011
Blakely, T   +3 more
core  

Obesity Prevalence in DDX3X‐Related Neurodevelopmental Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The purpose of this study is to analyze the prevalence of obesity in those affected by DDX3X‐related neurodevelopmental disorder (DDX3X‐NDD). Initial descriptions suggested that individuals with DDX3X‐NDD suffered from poor weight gain or failure to thrive in early childhood, likely in the setting of feeding difficulties and secondary to ...
Giavanna Verdi, Nathaniel H. Robin
wiley   +1 more source

Children With 22.Q.11.2 Deletion Syndrome: Sleep‐Disordered Breathing and Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Patients with 22q11.2 deletion syndrome (22q11DS) are predisposed to obstructive sleep apnea (OSA) due to an abnormal craniofacial anatomy with pharyngeal hypotonia, retrognathia, micrognathia, and glossoptosis. The aim of the study was to describe the prevalence and management of OSA in a cohort of children with 22q11DS.
Domenico Paolo La Regina   +6 more
wiley   +1 more source

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