Results 151 to 160 of about 70,455 (303)

Maximizing Neurovascular Outcomes of Facial Transplantation: A Comprehensive Review

Clinical Anatomy, Volume 39, Issue 8, Page 965-979, November 2026.
ABSTRACT Facial transplantation is a division of reconstructive surgery which aims to improve the function and appearance of a face that has endured severe disfigurement. Currently, the face transplant procedure uses allogenic tissue, harvested from a brain‐dead donor, to replace damaged facial components.
Olivia A. James, Faye Bennett
wiley   +1 more source

Systemic loxoscelism with hemolysis and positive Coombs: diagnostic and physiopathological implications. [PDF]

Rev Inst Med Trop Sao Paulo
Costa JA, Rocha LR, Andrade Filho A, Haddad CMSLD, Almeida JS.   +4 more
europepmc   +1 more source

Therapeutic Reversal of Severe Neuropsychiatric Symptoms in Wilson's Disease: A Case Report

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Wilsons disease is an autosomal recessive genetic disorder of copper metabolism that results in copper accumulation in liver and other organs. Hepatic manifestation tends to occur earlier than the neurological manifestation. We present a case with psychiatric presentation.
Tshering Penjor, Sangay Dorji, Sonam Wangchuk   +2 more
wiley   +1 more source

Persistence of antenatal anti-D immunoglobulin G at delivery in twin versus singleton pregnancies: a retrospective cohort study. [PDF]

BMC Pregnancy Childbirth
Ünlü C, Aksoy H.
europepmc   +1 more source

Primary Sjögren syndrome presenting with hemolytic anemia and pure red cell aplasia following delivery due to Coombs-negative autoimmune hemolytic anemia and hemophagocytosis.

Internal medicine, 2013
Y. Komaru, T. Higuchi, Ryosuke Koyamada, Y. Haji, M. Okada, T. Kamesaki, Sadamu Okada   +6 more
semanticscholar   +1 more source

Chronic Calcific Pancreatitis as the Probable Initial Manifestation of Systemic Lupus Erythematosus With Mixed Connective Tissue Disease Overlap: A Case Report

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Chronic calcific pancreatitis as the presenting manifestation of systemic lupus erythematosus (SLE) is exceedingly rare, particularly in tropical regions where it may be misattributed to tropical chronic pancreatitis (TCP). A 22‐year‐old Bangladeshi male farmer presented with a one‐year history of recurrent postprandial epigastric pain and ...
Rashid Shahriar Sazal, Abdullah Al Faisal, Sabiha Sikder, Moontasir Ahmed, Md. Riyaz Uddin Sk. Mubin, Sakin Saleh Ifti   +5 more
wiley   +1 more source

Systemic lupus erythematosus associated with paroxysmal nocturnal hemoglobinuria: a case report and literature review highlighting the clinical significance of small PNH clones. [PDF]

Front Immunol
Huang X, Huang J, Liu N, Zhang L.
europepmc   +1 more source

Australian Biography: Dr H.C. Nugget Coombs

Dr. H.C. "Nugget" Coombs, born in 1906, talks about all aspects of his career as an economist in Australia, including the years 1941-1975 during which time he served and advised seven prime ...
Interviewer: Robin Hughes, Heimans, Frank, Film Australia, Interviewee: Herbert Cole 'Nugget' Coombs (1906-1997)   +3 more
core  

INTERVIEW WITH ZOE COOMBS MARR

, 2019
INTERVIEW WITH ZOE COOMBS ...
Miles O'Neil (13084914)
core  

Successful Thromboembolectomy for PTE in an Adolescent Patient With Catastrophic APS and SLE

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT In a 14‐year‐old with antiphospholipid syndrome (APS) and lupus anticoagulant, improper switching from warfarin and low‐dose aspirin to rivaroxaban led to life‐threatening recurrent thrombosis, pulmonary embolism, and pulmonary hypertension. Prompt return to standard anticoagulation plus immunosuppression stabilized the condition.
Azadeh Zeinab Mirzaee, Bita Paknejad, Aziz Eghbali, Reza Shiari, Niku Rahimi Afzal   +4 more
wiley   +1 more source