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Respiratory failure in diabetic ketoacidosisDelayed diagnosis of Kearns-Sayre syndrome in a 38-year-old male patient: a case report.Kearns-Sayre syndrome: a case series of 35 adults and childrenEarly onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review.Genetic causes of hypomagnesemia, a clinical overviewCombined occurrence of diabetes mellitus and retinitis pigmentosa.Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure.Maternal transmission of diabetes.A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatmentEndocrine manifestations related to inherited metabolic diseases in adults.Kearns-Sayre syndrome: An unusual ophthalmic presentation.Kearns-Sayre syndrome presenting as isolated growth failure.Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELASEndocrine disorders in mitochondrial disease.Hypocalcemia in the critically ill patient.Kearns Sayre Syndrome--case report with review of literature.The eye as a window to rare endocrine disorders.Perspectives in Pediatric Pathology, Chapter 21. Testicular Pathology in Heritable Metabolic Disease.Triads in Ophthalmology: A Comprehensive Review.Mitochondrial disease and endocrine dysfunction.Ophthalmic clues to the endocrine disorders.Genetics of mitochondrial dysfunction and infertility.Risk factors for poor bone health in primary mitochondrial disease.Kearns Sayre Syndrome (KSS) - A Rare Cause For Cardiac Pacing.De Toni-Debré-Fanconi syndrome in a patient with Kearns-Sayre syndrome: a case report.Obstetric anesthesia considerations in Kearns-Sayre syndrome: a case report.Large mitochondrial DNA deletion in an infant with addison disease.Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism.Rare autosomal dominant POLG1 mutation in a family with metabolic strokes, posterior column spinal degeneration, and multi-endocrine disease.Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism.Anesthetic management of a parturient with Kearns-Sayre syndrome, dual-chamber and VVI implantable defibrillator pacemaker/defibrillator, and preeclampsia for cesarean delivery: A case report and review of the literature.Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome.Hypoparathyroidism.Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study.Endocrine disorders in two sisters affected by MELAS syndrome.Concurrent myopathy in patients with Graves' orbitopathy.Hypocalcemic myopathy without tetany due to idiopathic hypoparathyroidism: case report.Endocrine Disorders in Primary Mitochondrial Disease.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Endocrine dysfunction in Kearns-Sayre syndrome
@ast
Endocrine dysfunction in Kearns-Sayre syndrome
@en
Endocrine dysfunction in Kearns-Sayre syndrome
@nl
type
label
Endocrine dysfunction in Kearns-Sayre syndrome
@ast
Endocrine dysfunction in Kearns-Sayre syndrome
@en
Endocrine dysfunction in Kearns-Sayre syndrome
@nl
prefLabel
Endocrine dysfunction in Kearns-Sayre syndrome
@ast
Endocrine dysfunction in Kearns-Sayre syndrome
@en
Endocrine dysfunction in Kearns-Sayre syndrome
@nl
P2860
P1476
Endocrine dysfunction in Kearns-Sayre syndrome
@en
P2093
P2860
P304
P356
10.1111/J.1365-2265.1992.TB02289.X
P407
P577
1992-07-01T00:00:00Z