C Prehu
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Explore the profile of C Prehu including associated specialties, affiliations and a list of published articles.
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42
Citations
129
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Recent Articles
21.
Prehu C, Godart C, Vigneron C, Wajcman H
C R Acad Sci III
. 1998 Oct;
321(5):373-6.
PMID: 9766188
Three hemoglobin variants (Hb Nancy, Osler and Fort Gordon), carrying the same Tyr-->Asp substitution at position beta 145 (HC2), have been independently described in 1975 in patients with marked polycythemia....
22.
Lee K, Prehu C, Merault G, Keclard L, Roudot-Thoraval F, Bachir D, et al.
Am J Hematol
. 1998 Sep;
59(1):15-21.
PMID: 9723571
The clinical and biological heterogeneity of sickle cell hemoglobin (Hb) C disease (SC disease) is similar to sickle cell anemia, but has a much milder course. The effect of genetic...
23.
Bouanga J, Mouele R, Prehu C, Wajcman H, Feingold J, Galacteros F
Hum Hered
. 1998 Aug;
48(4):192-7.
PMID: 9694250
G6PD genotypes were determined in Brazzaville (Congo) on 188 HbSS patients (109 females, 79 males) and 210 controls (115 females and 95 males) with HbAA. DNA samples were analyzed by...
24.
Wajcman H, Prome D, Prehu C, Deon C, Riou J, Bouanga J, et al.
Hemoglobin
. 1998 May;
22(2):129-40.
PMID: 9576330
Hb Les Andelys [alpha83(F4)Leu-->Pro] is a mildly unstable variant that was found during glycated hemoglobin measurement in a French family. In this hemoglobin molecule the affected site, in the alpha...
25.
Wajcman H, Dahmane M, Prehu C, Costes B, Prome D, Arous N, et al.
Br J Haematol
. 1998 Mar;
100(2):401-6.
PMID: 9488635
Single point mutation, which accounts for 92% of the 700 known variants, is the most frequent genetic defect responsible for abnormal haemoglobins. Small deletions (or insertions) involving from one to...
26.
Wajcman H, Prehu M, Prehu C, Blouquit Y, Prome D, Galacteros F
Hum Mutat
. 1998 Feb;
Suppl 1:S20-2.
PMID: 9452028
No abstract available.
27.
Riou J, Godart C, Hurtrel D, Mathis M, Bimet C, Bardakdjian-Michau J, et al.
Clin Chem
. 1997 Jan;
43(1):34-9.
PMID: 8990219
A battery of relatively simple tests allows the presumptive identification of hemoglobin (Hb) variants, making unnecessary structural analysis by protein chemistry methods or DNA sequencing. The primary step in this...
28.
Wajcman H, DUCROCQ R, Riou J, Mathis M, Godart C, Prehu C, et al.
Anal Biochem
. 1996 May;
237(1):80-7.
PMID: 8660541
Human globin chain analysis provides important information on the genetics and molecular pathophysiology of hemoglobinopathies. We propose using perfusion chromatography on the reversed-phase stationary phase to perform these studies. The...
29.
Wajcman H, Blouquit Y, Lahary A, Soummer A, Groff P, Bardakdjian J, et al.
Hemoglobin
. 1995 Sep;
19(5):281-6.
PMID: 8537232
No abstract available.
30.
Wajcman H, Kister J, Prome D, Blouquit Y, Prehu C, Poyart C, et al.
C R Acad Sci III
. 1995 Jul;
318(7):785-94.
PMID: 7583766
Only 16 hemoglobin (Hb) variants carrying 2 point mutations within the same polypeptide chain have been identified up to now. Two of those are reported in this paper. In Hb...