✦ LIBER ✦

Type III hyperlipoproteinaemia and primary amenorrhoea associated with severe hypothyroidism

✍ Scribed by M Kršek; R Češka; A Hořinek; B Hořrejši; V Weiss

Book ID: 114812493
Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 68 KB
Volume: 89
Category: Article
ISSN: 0803-5253
DOI: 10.1111/j.1651-2227.2000.tb00429.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Increased serum creatinine associated wi

Increased serum creatinine associated with severe primary hypothyroidism

✍ C HALL; J BATCH; C JONES 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 134 KB

Expression of type III hyperlipoproteina

Expression of type III hyperlipoproteinaemia in a subject with secondary hypothyroidism bearing the apolipoprotein E2/2 phenotype

✍ G. FEUSSNER; R. ZIEGLER 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 265 KB

Acquired von Willebrand’s syndrome in a

Acquired von Willebrand’s syndrome in a patient with severe primary hypothyroidism associated with myasthenia gravis in the course of autoimmune polyglandular syndrome type 3

✍ M. LUBINSKA; R. SWIATKOWSKA-STODULSKA; E. KAZIMIERSKA; K. SWORCZAK 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 413 KB

Severe type III hyperlipoproteinemia ass

Severe type III hyperlipoproteinemia associated with unusual apolipoprotein E1 phenotype and & epsilon;1/lsquo;null genotype‡

✍ G. FEUSSNER; H. FUNKE; W. WENG; G. ASSMANN; K. J. LACKNER; R. ZIEGLER 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 948 KB

Congenital dyserythropoietic anemia type

Congenital dyserythropoietic anemia type III associated with congenital atrioseptal defect has led to severe cardiac problems in a 32-year-old patient

✍ G. Röhrig; H. Kilter; D. Beuckelmann; A. Kröner; C. Scheid; V. Diehl; D. Söhngen 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 708 KB

We report the case of a 32-year-old woman who was admitted at hospital because of ortho-dyspnea, arrhythmia, and paleness. Clinical examination showed continuous arrhythmia, systolic heart murmur, enlargement of spleen and liver, and pathologic hematological parameters, thus indicating an intravasal

Severe familial primary hypoalphalipopro

Severe familial primary hypoalphalipoproteinemia in French Canadian kindred: no association with the apo A-I/C-III/A-IV and A-II gene loci, normal LCAT activity, normal triglyceride levels and lack of clinical manifestations of Tangier Disease

✍ M. Marcil; B. Boucher; B.C. Solymos; J. Davignon; J. Frolich; J. Genest Jr 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 309 KB