A. Reghis: search on Z-Library

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1

The‐Asian‐learner‐as‐a‐rote‐learner Stereotype: myth or reality?

Watkins, David, Reghi, Murari, Astilla, Estela

Journal:

Educational Psychology

Year:

1991

Language:

english

File:

PDF, 795 KB

english, 1991

2

Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: First report of two cases

C. Junien, A. Leroux, D. Lostanlen, A. Reghis, J. Boue, H. Nicolas, A. Boue, J. C. Kaplan

Journal:

Prenatal Diagnosis

Year:

1981

Language:

english

File:

PDF, 462 KB

english, 1981

3

Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect?

Sepideh Akhavan, Ouerdia Chafa, Fatou Nsoure Obame, Marie-Françoise Torchet, Abderrezak Reghis, Anne-Marie Fischer, Jacqueline Tapon-Bretaudière

Journal:

European Journal of Haematology

Year:

2007

Language:

english

File:

PDF, 466 KB

english, 2007

4

A new TaqI allele at DXS52 frequent in Algeria

Nafa, K., Reghis, A., Benabadji, M., Delpech, M., Kaplan, J.C.

Journal:

Nucleic Acids Research

Year:

1989

Language:

english

File:

PDF, 40 KB

english, 1989

5

Quantitative variations of red-cell cytochrome b5reductase (NADH-methemoglobin-reductase) in the Algerian population

A. Reghis, M. Benabadji, P. Tchen, J. C. Kaplan

Journal:

Year:

1981

Language:

english

File:

PDF, 483 KB

english, 1981

6

Is the del521T mutation in the gamma-sarcoglycan gene a founder mutation in Mediterranean countries?

F. Leturcq, K. Azibi, F. Piccolo, N. Deburgrave, V. Marin, C. de Toma, M. Chaouch, A. Reghis, F. El Kerch, A. Sefiani, A. Sbiti, J-C. Kaplan, M. Jeanpierre

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 128 KB

english, 1997

7

Genetic and allelic heterogeneity of LGMD in North Africa

K. Azibi, M. Chaouch, A. Reghis, F. El Kerch, A. Sbiti, A. Sefiani, F. Leturcq, M. Jeanpierre, A. Carrié, F. Piccolo, C. Beldjord, J.-C. Kaplan

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 128 KB

english, 1997

8

Screening for mutations in factor VIII gene using the single-strand conformation polymorphism

Khédoudja Nafa, Farida Meriane, Thouraya Chellali, Mohamed Benabadji, Abderrezak Reghis, Michèle Viemont, Jean-Claude Kaplan, Marc Delpech

Journal:

Year:

1995

Language:

english

File:

PDF, 498 KB

english, 1995

9

Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X

Ouerdia Chafa, Madjid Tagzirt, Jacqueline Tapon-Bretaudière, Abderrezak Reghis, Anne-Marie Fischer, Bernard F. LeBonniec

Journal:

Thrombosis Research

Year:

2009

Language:

english

File:

PDF, 569 KB

english, 2009

10

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Piccolo, F., Roberds, S.L., Jeanpierre, M., Leturcq, F., Azibi, K., Beldjord, C., Carrié, A., Récan, D., Chaouch, M., Reghis, A.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 387 KB

1995

11

Characterization of weak alleles at the DIA1locus (Mustapha 1, Mustapha 2, and Mustapha 3) in the Algerian population

A. Reghis, C. Troungos, D. Lostanlen, R. Krishnamoorthy, J. C. Kaplan

Journal:

Year:

1983

Language:

english

File:

PDF, 301 KB

english, 1983

12

An Internally-Consistent Thermodynamics for Elastomers

Livingston, H. K., Reghi, G. P.

Journal:

Rubber Chemistry and Technology

Year:

1969

File:

PDF, 264 KB

1969

13

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria

Khedoudja Nafa, Abderrezak Reghis, Naima Osmani, Lamia Baghli, Hassen Aït-Abbes, Mohamed Benabadji, Jean-Claude Kaplan, Tom Vulliamy, Lucio Luzzatto

Journal:

Year:

1994

Language:

english

File:

PDF, 467 KB

english, 1994

14

G6PD Aures: a new mutation (48 lle → Thr) causing mild G6PD deficiency is associated with favism

Nafa, Khedoudja, Reghis, Abderrezak, Osmani, Naima, Baghli, Lamia, Benabadji, Mohamed, Kaplan, Jean-Claude, Vulliamy, Thomas J., Luzzatto, Lucio

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 581 KB

english, 1993

15

Prevalence of the Prothrombin Gene 20210A Mutation in Thrombophilic and Healthy Algerian Subjects

Helley, Dominique, Chafa, Ouerdia, Yaker, Najat Leila, Reghis, Abderrezak, Fischer, Anne-Marie

Journal:

Thrombosis and Haemostasis

Year:

1999

File:

PDF, 79 KB

1999

16

Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain

Keren Borensztajn, Ouerdia Chafa, Bernard Le Bonniec, Henri Wajcman, Abderrezak Reghis, Anne-Marie Fischer, Jacqueline Tapon-Bretaudière

Journal:

Thrombosis Research

Year:

2005

Language:

english

File:

PDF, 113 KB

english, 2005

17

Endogenous proteolysis of membrane-bound red cell cytochrome-b5 reductase in adults and newborns: its possible relevance to the generation of the soluble "methemoglobin reductase"

Choury, D, Reghis, A, Pichard, AL, Kaplan, JC

Journal:

Year:

1983

File:

PDF, 712 KB

1983

18

Homozygous nonsense mutation (Cys72→stop) in the human F7 gene: a not life-threatening mutation despite the absence of circulating factor VII

O. CHAFA, A-M. FISCHER, A. REGHIS, J. TAPON-BRETAUDIERE

Journal:

Journal of Thrombosis and Haemostasis

Year:

2005

Language:

english

File:

PDF, 96 KB

english, 2005

19

Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers

Chafa, O., Chellali, T., Sternberg, C., Reghis, A., Hamladji, R. M., Fischer, A. M.

Journal:

Blood Coagulation & Fibrinolysis

Year:

1995

File:

PDF, 338 KB

1995

20

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria

K. Nafa, F. Meriane, A. Reghis, M. Benabadji, F. Demenais, M. Guilloud-Bataille, Y. Sultan, J. C. Kaplan, M. Delpech

Journal:

Year:

1990

Language:

english

File:

PDF, 602 KB

english, 1990

21

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

Keren Borensztajn, Ouerdia Chafa, Martine Alhenc-Gelas, Siham Salha, Abderrezak Reghis, Anne-Marie Fischer, Jacqueline Tapon-Bretaudière

Journal:

British Journal of Haematology

Year:

2002

Language:

english

File:

PDF, 109 KB

english, 2002

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