H. Elghezal: search on Z-Library

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1

Place de l’échographie pelvienne réalisée par voie sus-pubienne dans l’exploration de l’insuffisance ovarienne prématurée

Braham, R., Hidar, S., Chaieb, M., Trimeche, S., Zaouali, M., Lakhal, B., Saâd, A., Ach, K., Chaieb, L., Elghezal, H.

Journal:

Annales d'Endocrinologie

Year:

2010

File:

PDF, 184 KB

2010

2

Assessment of chromosomal aberrations, micronuclei and proliferation rate index in peripheral lymphocytes from Tunisian nurses handling cytotoxic drugs

Sana Bouraoui, Aicha Brahem, Faten Tabka, Najib Mrizek, Ali Saad, Hatem Elghezal

Journal:

Environmental Toxicology and Pharmacology

Year:

2011

Language:

english

File:

PDF, 216 KB

english, 2011

3

Chromosomal Microarray Analysis in a Girl With Mental Retardation and Spina Bifida

Inesse Ben Abdallah, Hanene Hannachi, Najla Soyah, Ali Saad, Hatem Elghezal

Journal:

Pediatric Neurology

Year:

2011

Language:

english

File:

PDF, 580 KB

english, 2011

4

Semen processing by density gradient centrifugation is useful in selecting sperm with higher double-strand DNA integrity

S. Brahem, M. Mehdi, H. Elghezal, A. Saad

Journal:

Year:

2011

Language:

english

File:

PDF, 91 KB

english, 2011

5

Syndrome de Jacobsen : à propos d'un cas

A. Bedoui, H. Ben Hamouda, A. Ayadi, M. Braham, H. Soua, H. Elghezal, A. Saad, M.-T. Sfar

Journal:

Journal de Pédiatrie et de Puériculture

Year:

2005

Language:

french

File:

PDF, 176 KB

french, 2005

6

Screening for mutations of the FOXO4 gene in premature ovarian failure patients

Dora Janeth Fonseca, Eliana Garzón, Besma Lakhal, Rim Braham, Diego Ojeda, Hatem Elghezal, Ali Saâd, Carlos Martín Restrepo, Paul Laissue

Journal:

Reproductive BioMedicine Online

Year:

2012

Language:

english

File:

PDF, 162 KB

english, 2012

7

Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia

Abir Gmidène, Hlima Sennana, Hatem Elghezal, Sihem Ziraoui, Yosra Ben Youssef, Moez Elloumi, Lamia Issaoui, Imed Harrabi, Sophie Raynaud, Ali Saad

Journal:

Hematological Oncology

Year:

2008

Language:

english

File:

PDF, 212 KB

english, 2008

8

T(1;21;8)(p34;q22;q22): a novel variant of t(8;21) in acute myeloblastic leukemia with maturation

Abir Gmidène, Rim Frikha, Hlima Sennana, Hatem Elghezal, Moez Elloumi, Ali Saad

Journal:

Medical Oncology

Year:

2011

Language:

english

File:

PDF, 252 KB

english, 2011

9

Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients

B Lakhal, R Braham, R Berguigua, N Bouali, M Zaouali, M Chaieb, RA Veitia, A Saad, H Elghezal

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 558 KB

english, 2010

10

Semen Parameters and Sperm DNA Fragmentation as Causes of Recurrent Pregnancy Loss

Sonia Brahem, Meriem Mehdi, Hanène Landolsi, Soumaya Mougou, Hatem Elghezal, Ali Saad

Journal:

Year:

2011

Language:

english

File:

PDF, 236 KB

english, 2011

11

Cytogenetic and Molecular Aspects of Absolute Teratozoospermia: Comparison Between Polymorphic and Monomorphic Forms

Sonia Brahem, Hatem Elghezal, Houda Ghédir, Hanène Landolsi, Abdelbacett Amara, Samira Ibala, Moez Gribaa, Ali Saad, Meriem Mehdi

Journal:

Year:

2011

Language:

english

File:

PDF, 308 KB

english, 2011

12

P152 - Les marqueurs d’insulinorésistance et troubles métaboliques au cours du syndrome des ovaires polykystiques

S. Trimeche, M. Abid Safer, M. Chadli Chaieb, M. Zaouali Ajina, R. Braham Elghezal, A. Maaroufi Beizig, K. Ach, M. Kacem Njah, L. Chaieb

Journal:

Diabetes & Metabolism

Year:

2011

Language:

french

File:

PDF, 59 KB

french, 2011

13

PP-195. Supernumerary marker chromosome: A study about 47 perinatal cases

Dimassi Sarra, Mougou Soumaya, Mehri Souhir, Elghezal Hatem, Saad Ali

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 70 KB

english, 2010

14

Aneuploidy rate in spermatozoa of selected men with severe teratozoospermia

M. Mehdi, A. Gmidène, S. Brahem, J. F. Guerin, H. Elghezal, A. Saad

Journal:

Year:

2012

Language:

english

File:

PDF, 89 KB

english, 2012

15

735 Contribution of Alkylating Agents in the Cytogenetic Diagnosis of Fanconi Anemia

Bouraoui, S., Mougou, S., Mamai, O., Elghezal, H., Saad, A.

Journal:

Archives of Disease in Childhood

Year:

2012

Language:

english

File:

PDF, 590 KB

english, 2012

16

PP-196. The derivative 22 syndrome: A case report

Dimassi Sarra, Mougou Soumaya, Nouri Sonia, Elghezal Hatem, Saad Ali

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

17

738 Molecular Characterization of DER (8) (QTERQ21.13: PTERP23.3) Dn In a Child Associating Psychomotor Retardation, Hydrocephalus and Facial Dysmorphism

Hannachi, H., Mougou-Zerelli, S., Helal, K. B., Abdallah, I. B., Hmida, D., Elghezal, H., Saad, A.

Journal:

Archives of Disease in Childhood

Year:

2012

Language:

english

File:

PDF, 592 KB

english, 2012

18

DEM simulations of stiff and soft materials with crushable particles: an application of expanded perlite as a soft granular material

Elghezal, L., Jamei, M., Georgopoulos, I.-O.

Journal:

Granular Matter

Year:

2013

Language:

english

File:

PDF, 2.01 MB

english, 2013

19

PP-198. Isochromosome 18q: A cytogenetic study

Dimassi Sarra, Mougou Soumaya, Yacoubi Tahar, Fkih Meriem, Elghezal Hatem, Saad Ali

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 68 KB

english, 2010

20

Analyse génétique des insuffisances ovariennes prématurées : implication des gènes forkhead et TGF-β

B. Lakhal, P. Laissue, H. Elghèzal, M. Fellous

Journal:

Gynécologie Obstétrique & Fertilité

Year:

2008

File:

PDF, 220 KB

2008

21

Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR)

S. Hadiji Mseddi, L. Kammoun, H. Bellaaj, Y. Ben Youssef, L. Aissaoui, L. Torjemane, F. Telmoudi, A. Amouri, H. Elghezal, M. Ouederni, Y. Ben Abdennebi, S. Hammemi, T. Ben Othmen, H. Ben Abid, M. Beja

Journal:

Archives de Pédiatrie

Year:

2012

Language:

english

File:

PDF, 648 KB

english, 2012

22

PP-199. The Jacobsen syndrome: Tow cases report

Mougou Soumaya, Dimassi Sarra, Hannachi Hanene, Mellouli Fethi, Ben Hammouda Hechmi, Elghezal Hatem, Saad Ali

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 54 KB

english, 2010

23

Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome

Halima Sennana Sendi, Haifa Hichri, Hatem Elghezal, Moez Gribaa, Adnène Laatiri, Moez Elloumi, Raihane Ben Lakhal, Ali Saad

Journal:

Annales de Génétique

Year:

2002

Language:

english

File:

PDF, 53 KB

english, 2002

24

Prevalence of chromosomal abnormalities in couples with recurrent miscarriage

Hatem Elghezal, Samir Hidar, Soumaya Mougou, Hedi Khairi, Ali Saâd

Journal:

Fertility and Sterility

Year:

2007

Language:

english

File:

PDF, 64 KB

english, 2007

25

Corrigendum to “Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure” [Gene 509 (2012) 298–301]

Lakhal, Besma, Ben-Hadj-Khalifa, Sonia, Bouali, Nouha, Braham, Rim, Hatem, Elghezal, Saad, Ali

Journal:

Year:

2013

Language:

english

File:

PDF, 91 KB

english, 2013

26

PP-200. The antenatal diagnosis of chromosomal abnormalities: A Tunisian study about 10,944 cases

Dimassi Sarra, Mougou Soumaya, Fkih Meriem, Elghezal Hatem, Saad Ali

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 54 KB

english, 2010

27

Phenotype and Micro-array characterization of duplication 11q22.1-q25 and review of the literature

Ben-Abdallah-Bouhjar, Inesse, Mougou-Zerelli, Soumya, Hannachi, Hanene, Ben-Khelifa, Hela, Soyah, Najla, Labalme, Audrey, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

Journal:

Year:

2013

Language:

english

File:

PDF, 1.10 MB

english, 2013

28

Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia

Elghezal Hatem, Ben Rekaya Meriam, Denguezli Walid, Moussa Adenen, Gribaa Moez, Saad Ali

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 151 KB

english, 2007

29

Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia

Halima Sennana Sendi, Hatem Elghezal, Henda Temmi, Haifa Hichri, Moez Gribaa, Halima Elomri, Belkiss Meddeb, Tarek Ben Othmane, Moez Elloumi, Ali Saad

Journal:

Annales de Génétique

Year:

2002

Language:

english

File:

PDF, 51 KB

english, 2002

30

Clinical and Molecular Characterization of a Combined 17p13.3 Microdeletion with Partial Monosomy 21q21.3 in a 26-Year-Old Man

Hannachi, H., Mougou-Zerelli, S., BenAbdallah, I., Mama, N., Hamdi, I., Labalme, A., Elghezal, H., Sanlaville, D., Saad, A.

Journal:

Cytogenetic and Genome Research

Year:

2011

Language:

english

File:

PDF, 1.21 MB

english, 2011

31

De Novo CD5 Negative Blastic Mantle Cell Lymphoma Presented with Massive Bone Marrow Necrosis without Adenopathy or Organomegaly

Elyamany, Ghaleb, Alzahrani, Ali Matar, Al Mussaed, Eman, Aljasem, Hassan, Alotaibi, Sultan, Elghezal, Hatem

Journal:

Case Reports in Hematology

Year:

2015

Language:

english

File:

PDF, 4.09 MB

english, 2015

32

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia

Ben-Abdallah-Bouhjar, Inesse, Hannachi, Hanene, Labalme, Audrey, Gmidène, Abir, Mougou, Soumaya, Soyah, Najla, Gribaa, Moez, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

Journal:

European Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 469 KB

english, 2012

33

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits

Khelifa, Hela, Kammoun, Molka, Hannachi, Hanene, Soyah, Najla, Hammami, Saber, Elghezal, Hatem, Sanlaville, Damien, Saad, Ali, Mougou-Zerelli, Soumaya

Journal:

Journal of Pediatric Genetics

Year:

2015

Language:

english

File:

PDF, 3.59 MB

english, 2015

34

Detection of DNA fragmentation and meiotic segregation in human with isolated teratozoospermia

Sonia Brahem, Meriem Mehdi, Hatem Elghezal, Ali Saad

Journal:

Journal of Assisted Reproduction and Genetics

Year:

2011

Language:

english

File:

PDF, 202 KB

english, 2011

35

Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14)

Manel Mahjoub, Meriem Mehdi, Sonia Brahem, Hatem Elghezal, Samira Ibala, Ali Saad

Journal:

Journal of Assisted Reproduction and Genetics

Year:

2011

Language:

english

File:

PDF, 153 KB

english, 2011

36

A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure

Besma Lakhal, Paul Laissue, Rim Braham, Hatem Elghezal, Ali Saâd, Marc Fellous, Reiner A. Veitia

Journal:

Clinical Endocrinology

Year:

2009

Language:

english

File:

PDF, 411 KB

english, 2009

37

Array-CGH study of partial trisomy 9p without mental retardation

Inesse Ben Abdallah Bouhjar, Hanane Hannachi, Soumaya Mougou Zerelli, Audrey Labalme, Abir Gmidène, Najla Soyah, Sonia Missaoui, Damien Sanlaville, Hatem Elghezal, Ali Saad

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 877 KB

english, 2011

38

Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

Diego Ojeda, Besma Lakhal, Dora Janneth Fonseca, Rim Braham, Hanène Landolsi, Heidi Eliana Mateus, Carlos Martín Restrepo, Hatem Elghezal, Ali Saâd, Paul Laissue

Journal:

Fertility and Sterility

Year:

2011

Language:

english

File:

PDF, 219 KB

english, 2011

39

Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX

H. Ben Hamouda, N. Mkacher, H. Elghezal, H. Bannour, M. Kamoun, H. Soua, A. Saad, M.M. Souissi, M.T. Sfar

Journal:

Journal de Gynécologie Obstétrique et Biologie de la Reproduction

Year:

2009

File:

PDF, 497 KB

2009

40

The effects of male aging on semen quality, sperm DNA fragmentation and chromosomal abnormalities in an infertile population

Sonia Brahem, Meriem Mehdi, Hatem Elghezal, Ali Saad

Journal:

Journal of Assisted Reproduction and Genetics

Year:

2011

Language:

english

File:

PDF, 243 KB

english, 2011

41

Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders

Hatem Elghezal, Samir Hidar, Rim Braham, Walid Denguezli, Mounir Ajina, Ali Saâd

Journal:

Fertility and Sterility

Year:

2006

Language:

english

File:

PDF, 73 KB

english, 2006

42

Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation

Ben Khelifa, Hela, Soyah, Najla, Ben-Abdallah-Bouhjar, Inesse, Gritly, Ryma, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali, Mougou-Zerelli, Soumaya

Journal:

Year:

2013

Language:

english

File:

PDF, 981 KB

english, 2013

43

ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia

Gmidène, Abir, Elghezal, Hatem, Sennana, Hlima, Ben Youssef, Yosra, Meddeb, Balkiss, Elloumi, Moez, Khlif, Abderrahim, Saad, Ali

Journal:

Advances in Hematology

Year:

2009

Language:

english

File:

PDF, 581 KB

english, 2009

44

Cytogenetic Profile and FLT3 Gene Mutations of Childhood Acute Lymphoblastic Leukemia

Alkhayat, Nawaf, Elborai, Yasser, Al Sharif, Omer, Al Shahrani, Mohammad, Alsuhaibani, Omar, Awad, Mohammed, Elghezal, Hatem, ben-abdallah Bouhajar, Inesse, Alfaraj, Mona, Al Mussaed, Eman, Alabbas, F

Journal:

Clinical Medicine Insights Oncology

Year:

2017

Language:

english

File:

PDF, 175 KB

english, 2017

45

BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

Besma Lakhal, Paul Laissue, Rim Braham, Hatem Elghezal, Ali Saâd, Marc Fellous, Reiner A. Veitia

Journal:

Clinical Endocrinology

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

46

Large duplication 4q25–q34 with mild clinical effect

Hatem Elghezal, Halima Sennana Sendi, Kamel Monastiri, Jean Michel Lapierre, Samira Ibala Romdhane, Soumaya Mougou, Ali Saad

Journal:

Annales de Génétique

Year:

2004

Language:

english

File:

PDF, 121 KB

english, 2004

47

Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

D. H'mida, M. Gribaa, T. Yacoubi, A. Chaieb, L. Adala, H. Elghezal, A. Saad

Journal:

Year:

2008

Language:

english

File:

PDF, 2.03 MB

english, 2008

48

A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers

Bouraoui, Sana, Mougou, Soumaya, Drira, Afef, Tabka, Faten, Bouali, Nouha, Mrizek, Najib, Elghezal, Hatem, Saad, Ali

Journal:

International Journal of Occupational Medicine and Environmental Health

Year:

2013

Language:

english

File:

PDF, 478 KB

english, 2013

49

The oedometric compression behavior of expanded clay including the crushability of single particles

Ben Jamaa, Haithem, Elghezal, Latifa, Jamei, Mehrez

Journal:

Granular Matter

Year:

2020

Language:

english

File:

PDF, 1.56 MB

english, 2020

50

Prenatal diagnosis and characterization of an analphoid marker chromosome 16

A. C. Tabet, P. Gosset, H. Elghezal, S. Fontaine, J. Martinovic, F. Encha Razavi, S. Romana, M. Vekemans, N. Morichon-Delvallez

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 209 KB

english, 2004

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