✦ LIBER ✦

Hereditary Ring Sideroblastic Anaemia and Christmas Disease in a Swedish Family

✍ Scribed by Hast, R. ;Miale, T. ;Westin, J. ;Birgegård, G. ;Möller, E. ;Reizenstein, P. ;Teger-Nilsson, A.-C. ;Wetterberg, L.

Book ID: 114789999
Publisher: Wiley (Blackwell Publishing)
Year: 2009
Weight: 414 KB
Volume: 30
Category: Article
ISSN: 0036-553X
DOI: 10.1111/j.1600-0609.1983.tb02532.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Hereditary sideroblastic anaemia and aut

Hereditary sideroblastic anaemia and autosomal inheritance of erythrocyte dimorphism in a Dutch family

✍ G. D. van Waveren Hogervorst; H. P. C. van Roermund; P. J. Snijders 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 336 KB

Lack of efficacy of pyridoxine (vitamin

Lack of efficacy of pyridoxine (vitamin B6) treatment in acquired idiopathic sideroblastic anaemia, including refractory anaemia with ring sideroblasts

✍ Lisa M. Baumann Kreuziger; Alexandra P. Wolanskyj; Curtis A. Hanson; David P. St 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 80 KB

Molecular detection of carriers of hered

Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family

✍ Wallace, Margaret R. ;Conneally, P. Michael ;Long, George L. ;Benson, Merrill D. 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 535 KB

Identification of an arginine452 to hist

Identification of an arginine452 to histidine substitution in the erythroid 5-aminolaevulinate synthetase gene in a large pedigree with X-linked hereditary sideroblastic anaemia

✍ A. J. Edgar; M. S. Losowsky; J. S. Noble; Professor S. N. Wickramasinghe 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 473 KB

Haemolytic Disease of the Newborn and Ch

Haemolytic Disease of the Newborn and Chronic Anaemia Induced by γβ Thalassaemia in a Dutch Family

✍ M. Oort; W. Heerspink; D. Roos; R. A. Flavell; L. F. Bernini 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 928 KB

Combined hereditary factor XI (plasma th

Combined hereditary factor XI (plasma thromboplastin antecedent) deficiency, von Willebrand's disease, and xeroderma pigmentosum in a Japanese family

✍ Masayuki Sano; Hidehiko Saito; Yoshinori Shimamoto; Isamu Sugiura; Haruhiko Ohts 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 369 KB 👁 2 views

## H.S., I.S.) Japan We report a 28-year-old-Japanese male who had a skin tumor derived from variant type xeroderma pigmentosum (XP), combined with factor XI (FXI) deficiency and type llB von Willebrand's disease (vWd). The patient had abnormal bleeding history on tooth extraction. FXI clotting ac