𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Hexokinase Deficiency in Erythrocytes: A New Variant in 5 Members of a Finnish Family

✍ Scribed by Siimes, Martti A. ;Rahiala, Eeva-Liisa ;Leisti, Jaakko

Book ID
114789379
Publisher
Wiley (Blackwell Publishing)
Year
2009
Weight
320 KB
Volume
22
Category
Article
ISSN
0036-553X

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Glucosephosphate isomerase deficiency, a
Glucosephosphate isomerase deficiency, a new variant in a dutch family
✍ J. J. Rotteveel; G. A. M. Vaan; G. E. J. Staal; J. P. G. M. Biervliet; E. D. A. πŸ“‚ Article πŸ“… 1977 πŸ› Springer 🌐 English βš– 561 KB

The clinical course and the biochemical findings are reported from a patient suffering from glucosephosphate isomerase (G.P.I. EC 5.3.1.9) deficiency type Nijmegen. This disorder decleares itself as a non-spherocytic hemolytic anemia, presenting in the neonatal period. In the patient hemolysis was o

A functional deficiency of C1q in 3 fami
A functional deficiency of C1q in 3 family members
✍ A.J. Hannema; H.C. Kluin-Nelemans; C.E. Hack; C. MallΓ©e; H.P.T. van Helden; A.J. πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 English βš– 121 KB
G-6PD β€œankara”. A new G-6PD variant with
G-6PD β€œankara”. A new G-6PD variant with deficiency found in a Turkish family
✍ Axel Kahn; M. L. North; J. Messer; P. Boivin πŸ“‚ Article πŸ“… 1975 πŸ› Springer 🌐 English βš– 317 KB

A new G-6PD varient with enzyme deficiency is described in a 7-month-old Turkish boy without any hemolytic manifestation, except neonatal hyperbilirubinemia. The main characteristics of this variant were the following: Severe enzyme deficiency in erythrocytes (8% of normal), fast starch-gel-electrop