Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child

scientific article

Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child is …
instance of (P31):
scholarly articleQ13442814
case reportQ2782326

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P6179Dimensions Publication ID1008934892
P356DOI10.1186/1824-7288-38-49
P8608Fatcat IDrelease_u5zndbqmcjeznncr4rpsx434se
P932PMC publication ID3481365
P698PubMed publication ID22995124
P5875ResearchGate publication ID230893663

P50authorClaudio PignataQ30512461
Loredana PalamaroQ42780158
P2093author name stringDonatella Capalbo
Giustina Russo
Ida D'Acunzo
Maria Alessio
Mariacarolina Salerno
Nicola Improda
P2860cites workAdrenal involvement in the antiphospholipid syndrome: clinical and immunologic characteristics of 86 patientsQ28195403
International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS)Q28292418
Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patientsQ33341941
Clinical update on the management of adrenal hemorrhageQ33396589
Adrenal insufficiencyQ34203208
Autoimmune adrenal insufficiency and autoimmune polyendocrine syndromes: autoantibodies, autoantigens, and their applicability in diagnosis and disease predictionQ34671679
Antiphospholipid syndrome: multiple mechanismsQ35775322
Acute adrenal failure as the heralding symptom of primary antiphospholipid syndrome: report of a case and review of the literatureQ36270282
Adrenal insufficiency: still a cause of morbidity and death in childhoodQ36714931
Antiphospholipid syndrome in childrenQ37242374
Presentation of primary adrenal insufficiency in childhoodQ37862462
Severe combined immunodeficiences: new and old scenariosQ37976472
Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescenceQ46202462
Antipituitary antibodies recognizing growth hormone (GH)-producing cells in children with idiopathic GH deficiency and in children with idiopathic short statureQ48580085
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndromeQ58800395
Comparative Evaluation of Therapy with L -Thyroxine versus No Treatment in Children with Idiopathic and Mild Subclinical HypothyroidismQ60225569
Linear growth and intellectual outcome in children with long-term idiopathic subclinical hypothyroidismQ60225625
Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relatives.Q64964910
The antiphospholipid syndromeQ77739053
High intrafamilial variability in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: a case studyQ82446902
Acute adrenal insufficiency in a neonate with bilateral adrenal hemorrhage and combined prothrombotic risk factorsQ84264818
The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-upQ85058311
P407language of work or nameEnglishQ1860
P921main subjectantiphospholipid syndromeQ582207
adrenal crisisQ4057453
primary antiphospholipid syndromeQ63878006
P304page(s)49
P577publication date2012-09-20
P1433published inItalian Journal of PaediatricsQ15762169
P1476titleAcute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child
P478volume38

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