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1
Gene Expression in the Central Nervous System
~1~=!urv—' '-mu 13.3 132 113.1 1i—- - 11 12 / Po—_[ q 24 25 Gaucher disease,
type I Elllp'tocytoses—2 31 Spherocytoses, |"ecess1ve 3 2.1 322 Glycogenosns
III 32-3 41 42.1 _ , 355 CR1 clefnciency 43 44 _ Hypothyroidism, nongoitrous ...
2
100+ Clinical Cases In Paediatrics
The causes of spherocytoses are all of the following except (a) thermal injury (b)
drowning (c) septicaemia (d) Wilson's disease 10. The absolute indication of
splenectomy include all of the following except (a) severe anemia (b)
hepatomegaly ...
3
Vital Statistics of the United States
... not elsewhere classified (261.3) Pnaieevdeficiency anemia (291.4) - Anemia
associated with other specified nutritional deficiency (291.8) Unspecified (291.9)
hssssosawy hensolybc anensea (262) — - - Hereditary spherocytoses (262 0) ...
4
Advances in Parasitology
Spherocytoses 50: 5 Spheroides maculatus 36: 148 Sphingomyelin synthase 41:
36 Spike sensilla. gyrodactylids 44: 195, 197 Spilanthes oleraceae 50: 257
Spines of helminths, amino acids 30: 42 Spinning Enhanced Visible and Infrared
...
J. R. Baker, Ralph Muller, D. Rollinson, 2003
5
Red Cell Membrane Transport in Health and Disease
1996; certain human hereditary spherocytoses: Bruce and Tanner 1999). or
experimental genetic manipulation (knockout mice: Southgate et al. 1996). These
models provide the opportunity to investigate the correlation between band 3, ...
Ingolf Bernhardt, J. Clive Ellory, 2003
6
Mendeleev Chemistry Journal
... (insufficient activity of these enzymes produces different types of "congenital
nonspherocytic hemolytic anemias," which differ from hereditary spherocytoses,
thalassemias, hemolytic hereditary eliptocytoses, and hemoglobinopathies and
are ...
7
Clinical Laboratory Methods
... fragility mechanical, 136 spherocytoses, 209 G-6-PD deficiency, 210 Hb C, 114
Hb C disease, 1 1 5 hemoglobin content. 176 hemolysis, changes, 136 hemolytic
anemias, 208 inclusions. 183, 184, 213 Hb C disease, 213 Hb H, 118, 119 ...
John D. Bauer, Philip Gulick Ackermann, Gelson Toro, 1974
8
Clinical Genetics: A Short Course
Cytoskeletal proteins may be disrupted by genetic diseases such as the
spherocytoses (182870; Fig. 6.6). Spherocytosis can be diagnosed from blood
smears by noting small, round erythrocytes that are more rapidly destroyed.
Several types ...
9
Diagnosis in paediatric haematology
Other non-immune spherocytoses (see also Table 3.6) Spherocytosis may occur
in: • Envenomation (snakes, spiders, bees, wasps, jellyfish). Infrequent. Due to
direct membrane damage, intravascular coagulation or rarely immune effect ...
We have shown that deficiencies of ankyrin, a-spectrin and ft-spec- trin cause
hereditary spherocytoses in the mouse, preceding similar findings in the human
patients. Gene replacement is a putative treatment for diseases of the
hematopoietic ...
