Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A rare case of renal involvement in Lecithin-Cholesterol Acyltransferase (LCAT) deficiency: lessons for the clinical nephrologist.

  • Authors : Rath A; Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Bibinagar (Hyderabad Metropolitan Region), India. .; Zahir Z

  • Source: Journal of nephrology [J Nephrol] 2023 Mar; Vol. 36 (2), pp. 319-321. Date of Electronic Publication: 2022 Sep 26.Publisher: Springer Country of Publication: Italy NLM ID: 9012268 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1724-6059

Record details

×
Academic Journal

Familial LCAT deficiency and cardiovascular disease: the game is not over. A case of dramatic multivessel atherosclerosis.

  • Authors : Bigazzi F; Lipoapheresis Unit, Reference Center for the Diagnosis and Treatment of Inherited Dyslipidemias, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy.; Dal Pino B

  • Source: Minerva medica [Minerva Med] 2023 Aug; Vol. 114 (4), pp. 535-537. Date of Electronic Publication: 2020 May 29.Publisher: Edizioni Minerva Medica Country of Publication: Italy NLM ID: 0400732 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

Two Cases of Acquired High-Density Lipoprotein Deficiency with Immunoglobulin G4-Related Lecithin-Cholesterol Acyltransferase Autoantibody.

  • Authors : Komatsu T; Division of Anti-aging and Vascular Medicine, Department of Internal Medicine, National Defense Medical College.; Research Institute for Physical Activity, Fukuoka University.

  • Source: Journal of atherosclerosis and thrombosis [J Atheroscler Thromb] 2023 Aug 01; Vol. 30 (8), pp. 1070-1082. Date of Electronic Publication: 2022 Nov 16.Publisher: Japan Atherosclerosis Society Country of Publication: Japan NLM ID: 9506298 Publication Model: Print-Electronic Cited Medium: Internet

Record details

×
Academic Journal

Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges.

  • Source: Current opinion in lipidology [Curr Opin Lipidol] 2023 Apr 01; Vol. 34 (2), pp. 35-43. Date of Electronic Publication: 2022 Dec 06.Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9010000 Publication Model: Print-Electronic Cited Medium: Internet

Record details

×
Report

Clinical Dilemma of Corneal Opacity, Very Low High-density Lipoprotein, and Nephrotic Syndrome: Mystery Revealed.

  • Authors : Raina R; Department of Nephrology, Akron General Medical Center; Department of Nephrology, Akron Children's Hospital, Akron, OH, USA.

  • Source: Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia [Saudi J Kidney Dis Transpl] 2022 Mar-Apr; Vol. Publisher: Medknow Country of Publication: Saudi Arabia NLM ID: 9436968 Publication Model: Print Cited Medium: Internet ISSN: 1319-2442 (Print)

Record details

×
Academic Journal

Rapidly progressive renal failure to reveal LCAT deficiency in an Algerian family.

  • Source: Clinical nephrology [Clin Nephrol] 2023 Feb; Vol. 99 (2), pp. 92-97.Publisher: Dustri-Verlag Dr. Karl Feistle Country of Publication: Germany NLM ID: 0364441 Publication Model: Print Cited Medium: Internet ISSN:

Record details

×
Report

Administration of the High-Density Lipoprotein Mimetic CER-001 for Inherited Lecithin-Cholesterol Acyltransferase Deficiency.

  • Authors : Faguer S; Département de Néphrologie et Transplantation d'organes, Centre de Référence des Maladies Rénales Rares, Centre Hospitalier Universitaire de Toulouse, Institut National de la Science et de la Recherche Médicale, INSERM U1297-Institut des Maladies Métaboliques et Cardiovasculaires, and Université Paul Sabatier-Toulouse III, Toulouse, France.; Colombat M

  • Source: Annals of internal medicine [Ann Intern Med] 2021 Jul; Vol. 174 (7), pp. 1022-1025. Date of Electronic Publication: 2021 Mar 02.Publisher: American College of Physicians--American Society of Internal Medicine Country of Publication: United States NLM ID: 0372351 Publication Model:

Record details

×
Academic Journal

A novel pathogenic variant in LCAT causing FLD. A case report.

  • Authors : Goñi Ros N; Department of Clinical Biochemistry and Clinical Genetics, Hospital Universitario Miguel Servet, Zaragoza, Spain.; González-Tarancón R

  • Source: Acta clinica Belgica [Acta Clin Belg] 2022 Dec; Vol. 77 (6), pp. 970-975. Date of Electronic Publication: 2021 Nov 18.Publisher: Taylor & Francis Country of Publication: England NLM ID: 0370306 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.

  • Authors : Mehta R; Department of Endocrinology and Metabolism, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Av. Vasco de Quiroga 15, Belisario Domínguez Secc. 16, , Tlalpan, 14080, México City, México.; Elías-López D

  • Source: Lipids in health and disease [Lipids Health Dis] 2021 Jul 13; Vol. 20 (1), pp. 70. Date of Electronic Publication: 2021 Jul 13.Publisher: BioMed Central Country of Publication: England NLM ID: 101147696 Publication Model: Electronic Cited Medium: Internet ISSN: 1476-511X

Record details

×
Academic Journal

A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency.

  • Authors : Takeda T; Department of Endocrinology and Diabetology, Anjo Kosei Hospital, 28 Higashihirokute, Anjo, Aichi 446-8602, Japan (Drs Takeda, Ide, and Mizutani).; Ide T

  • Source: Journal of clinical lipidology [J Clin Lipidol] 2022 Jul-Aug; Vol. 16 (4), pp. 423-433. Date of Electronic Publication: 2022 Jun 17.Publisher: Elsevier Country of Publication: United States NLM ID: 101300157 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
  • 1-10 of  1,427 results for ""LECITHIN""