𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Patient with Pyruvate Carboxylase Deficiency in the Liver: Treatment with Aspartic Acid and Thiamine

✍ Scribed by M. G. Baal; F. J. M. Gabreëls; W. O. Renter; F. A. Hommes; Th. H. J. Gijsbers; K. J. B. Lamers; J. C. N. Kok

Book ID
115264122
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
597 KB
Volume
23
Category
Article
ISSN
0012-1622

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Ineffective erythropoiesis in the spleen
Ineffective erythropoiesis in the spleen of a patient with pyruvate kinase deficiency
✍ Shin Aizawa; Urara Kohdera; Masaki Hiramoto; Yutaka Kawakami; Ken-ichi Aisaki; Y 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 147 KB 👁 2 views

## Abstract In this study, possible adverse effects of pyruvate kinase (PK) deficiency on the maturation of erythroid progenitors were investigated. A 4‐year‐old Japanese girl with severe PK deficiency underwent splenectomy to reduce her need for blood transfusions. The spleen was examined a histol

Pyruvate carboxylase deficiency: Prenata
Pyruvate carboxylase deficiency: Prenatal onset of ischemia-like brain lesions in two sibs with the acute neonatal form
✍ Brun, Nathalie; Robitaille, Yves; Grignon, Andr�e; Robinson, Brian H.; Mitchell, 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 67 KB 👁 2 views

Pyruvate carboxylase (PC) is a key enzyme in the gluconeogenesis and anaplerotic metabolic pathways. PC deficiency is a rare autosomal recessive disorder with three clinical presentations: an infantile form, a severe neonatal form, and a benign form. We report brother and sister sibs with the severe