✦ LIBER ✦

Gilbert's syndrome co-existing with and masking hereditary spherocytosis

✍ Scribed by S. Sharma; S. J. Vukelja; S. Kadakia

Book ID: 105990267
Publisher: Springer
Year: 1997
Tongue: English
Weight: 150 KB
Volume: 74
Category: Article
ISSN: 0939-5555
DOI: 10.1007/s002770050302

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Severe hyperbilirubinemia in a 10-year-o

Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome

✍ KENICHI SUGITA; YOSHIHIRO MARUO; HIDEMITSU KUROSAWA; AKIRA TSUCHIOKA; TOSHIO FUJ 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 100 KB

Human papillomavirus with co-existing vu

Human papillomavirus with co-existing vulvar vestibulitis syndrome and vestibular papillomatosis

✍ M Origoni; M Rossi; D Ferrari; F Lillo; A.G Ferrari 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 133 KB

Symptoms and pathophysiological mechanis

Symptoms and pathophysiological mechanisms in patients with co-existing functional dyspepsia and irritable bowel syndrome

✍ M. Corsetti; P. Caenepeel; J. Janssens; J. Tack 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 132 KB

Co-existing point mutations of mitochond

Co-existing point mutations of mitochondrial DNA in a patient with a heart abnormality and Pearson syndrome-like symptoms

✍ Kae Munakata; Miki Bundo; Tadafumi Kato; Hiroaki Ono; Nobuo Sakura; Minoru Oosak 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 147 KB 👁 1 views

Frequent co-occurrence of the TATA box m

Frequent co-occurrence of the TATA box mutation associated with Gilbert’s syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians

✍ Christoph Köhle; Bernd Möhrle; Peter A. Münzel; Matthias Schwab; Dorothee Wernet 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 131 KB