K. Ouldim: search on Z-Library

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1

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

E. Bal, L. Baala, C. Cluzeau, F. El Kerch, K. Ouldim, S. Hadj-Rabia, C. Bodemer, A. Munnich, G. Courtois, A. Sefiani, A. Smahi

Journal:

Year:

2007

Language:

english

File:

PDF, 276 KB

english, 2007

2

Microdélétion 22q11.2 révélée par une hypocalcémie néonatale avec une dysmorphie faciale mineure

Siham Chafai Elalaoui, Ilham Ratbi, Souad Cherkaoui Deqaqi, Karim Ouldim, Abdelaziz Sefiani

Journal:

Revue Francophone des Laboratoires

Year:

2009

Language:

french

File:

PDF, 193 KB

french, 2009

3

Omenn Syndrome with Mutation inRAG1Gene

I. Cherkaoui Jaouad, K. Ouldim, S. Ali Ou Alla, Y. Kriouile, A. Villa, A. Sefiani

Journal:

Indian Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 292 KB

english, 2008

4

Multiple synostosis syndrome

Hicham Hachimi, Latifa Tahiri, Najoua Ghani, Karim Ouldim, Taoufik Harzy

Journal:

Joint Bone Spine

Year:

2012

Language:

english

File:

PDF, 327 KB

english, 2012

5

La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc

I. Ratbi, S. Hajji, K. Ouldim, N. Aboussair, D. Feldmann, A. Sefiani

Journal:

Archives de Pédiatrie

Year:

2007

Language:

french

File:

PDF, 241 KB

french, 2007

6

Unexpected fertility and paternal UPD 22

Karim Ouldim, Aziza Sbiti, Abdelbafid Natiq, Fatiha El-Kerch, Souad Cherkaoui, Abdelaziz Sefiani

Journal:

Fertility and Sterility

Year:

2008

Language:

english

File:

PDF, 92 KB

english, 2008

7

The first mutations in the MYH gene reported in Moroccan colon cancer patients

F.Z. Laarabi, I. Cherkaoui Jaouad, S. Baert-Desurmont, K. Ouldim, A. Ibrahimi, N. Kanouni, T. Frebourg, A. Sefiani

Journal:

Year:

2012

Language:

english

File:

PDF, 275 KB

english, 2012

8

Maladie des synostoses multiples

Hicham Hachimi, Latifa Tahiri, Najoua Ghani, Karim Ouldim, Taoufik Harzy

Journal:

Revue du Rhumatisme

Year:

2012

Language:

french

File:

PDF, 231 KB

french, 2012

9

Consanguinité et prédisposition aux néphropathies dans la population marocaine (à propos de 265 cas)

S. Jaafour, G. El Bardai, N. Kabbali, M.A. Lazrak, L. Bougennouch, I. Samri, M. Arrayhani, K. Ouldim, T. Sqalli

Journal:

Néphrologie & Thérapeutique

Year:

2012

Language:

french

File:

PDF, 47 KB

french, 2012

10

Improving medical research in the Arab world

El-Azami-El-Idrissi, Mohammed, Lakhdar-Idrissi, Mounia, Ouldim, Karim, Bono, Wafaa, Amarti-Riffi, Afaf, Hida, Moustapha, Nejjari, Chakib

Journal:

Year:

2013

Language:

english

File:

PDF, 50 KB

english, 2013

11

Prévalence de la mutation 35delG dans les surdités génétiques autosomiques récessives non syndromiques au Maroc

Taybi, Z., Ridal, M., Ouattassi, N., Bouloiz, R., Barakat, H., Ouldim, K., El Amine El Alami, N.

Journal:

Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale

Year:

2012

Language:

french

File:

PDF, 56 KB

french, 2012

12

TPMT alleles in the Moroccans

Janati Idrissi, Meryem, Samri, Imane, Khabbal, Youssef, El Hassouni, Mohammed, Ouldim, Karim

Journal:

Clinics and Research in Hepatology and Gastroenterology

Year:

2015

Language:

english

File:

PDF, 298 KB

english, 2015

13

L’exploration moléculaire du gène NKX2.5 dans deux populations atteintes de communication inter-auriculaire (CIA) et de tétralogie de Fallot (TOF)

El Bouchikhi, I., Belhassan, K., Moufid, F.Z., Houssaini, M.I., Atmani, S., Bouguenouch, L., Samri, I., Ouldim, K.

Journal:

Revue d'Épidémiologie et de Santé Publique

Year:

2015

Language:

french

File:

PDF, 163 KB

french, 2015

14

Caractérisation épidémiologique de la communication interventriculaire (CIV) dans la population marocaine

El Bouchikhi, I., Ouldim, K., Moufid, F.Z., Houssaini, M.I., Atmani, S.

Journal:

Revue d'Épidémiologie et de Santé Publique

Year:

2015

Language:

french

File:

PDF, 217 KB

french, 2015

15

The first PTPN11 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies

EL BOUCHIKHI, Ihss, SAMRI, Im, IRAQUI HOUSSAINI, Mohammed, TRHANINT, Saaid, BOUGUENOUCH, Laila, SAYEL, Hanane, HIDA, Moustapha, ATMANI, Samir, OULDIM, Karim

Journal:

TURKISH JOURNAL OF MEDICAL SCIENCES

Year:

2015

Language:

english

File:

PDF, 154 KB

english, 2015

16

Gonadal Dysgenesis 46, XX Associated with Mayer-Rokitansky-Kuster-Hauser Syndrome: One Case Report

Bousfiha, N., Errarhay, S., Saadi, H., Ouldim, K., Bouchikhi, C., Banani, A.

Journal:

Obstetrics and Gynecology International

Year:

2010

Language:

english

File:

PDF, 1.28 MB

english, 2010

17

Epigenetics could explain some Moroccan population colorectal cancers peculiarities: microsatellite instability pathway exploration

Sekal, Mohammed, Ameurtesse, Hassania, Chbani, Laila, Ouldim, Karim, Bennis, Sanae, Abkari, Mohammed, Boulouz, Amal, Benajah, Dafr Allah, Benjelloun, Basher, Ousadden, Abdelmalek, Ait Taleb, Khalid, A

Journal:

Diagnostic Pathology

Year:

2015

Language:

english

File:

PDF, 2.33 MB

english, 2015

18

The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family

Mejtoute, Touhami, Sayel, Hanane, El-Akhal, Jamila, Moufid, Fatima Z., Bouguenouch, Laila, El Bouchikhi, Ihssane, Hida, Mustapha, Couissi, Driss, Ouldim, Karim

Journal:

Human Genome Variation

Year:

2017

Language:

english

File:

PDF, 251 KB

english, 2017

19

Genetics and genomic medicine in Morocco: the present hope can make the future bright

Belhassan, Khadija, Ouldim, Karim, Sefiani, Abdel Aziz

Journal:

Molecular Genetics & Genomic Medicine

Year:

2016

Language:

english

File:

PDF, 795 KB

english, 2016

20

Gut microbiome of Moroccan colorectal cancer patients

Allali, Imane, Boukhatem, Noureddine, Bouguenouch, Leila, Hardi, Hanaa, Boudouaya, H. Abir, Cadenas, M. Belen, Ouldim, Karim, Amzazi, Saaïd, Azcarate-Peril, M. Andrea, Ghazal, Hassan

Journal:

Medical Microbiology and Immunology

Year:

2018

Language:

english

File:

PDF, 1.25 MB

english, 2018

21

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder

Ouldim, Karim, Natiq, Abdelhafid, Jonveaux, Philippe, Sefiani, Abdelaziz

Journal:

Journal of Biomedicine and Biotechnology

Year:

2007

Language:

english

File:

PDF, 1.62 MB

english, 2007

22

Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations

Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, El Otmani, Ihssane, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha

Journal:

Pan African Medical Journal

Year:

2017

File:

PDF, 429 KB

2017

23

Syndrome de Lynch: à propos d’un cas et revue de la litterature

Bouguenouch, Laila, Samri, Imane, Belhassan, Khadija, Sayel, Hanane, Abbassi, Meriame, Bennis, Sanae, Allah, Dafr, Ibrahimi, Adil, Amarti, Afaf, Ouldim, Karim

Journal:

Pan African Medical Journal

Year:

2016

File:

PDF, 151 KB

2016

24

Marqueurs chromosomiques: à propos d'un cas

Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Omairi, Nissrine El, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim

Journal:

Pan African Medical Journal

Year:

2013

Language:

french

File:

PDF, 433 KB

french, 2013

25

The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence

Moufid, Fatima Zahra, Bouguenouch, Laila, El Bouchikhi, Ihssane, Chbani, Laila, Iraqui Houssaini, Mohamed, Sekal, Mohamed, Belhassan, Khadija, Bennani, Bahia, Ouldim, Karim

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2018

Language:

english

File:

PDF, 257 KB

english, 2018

26

Agénésie bilatérale des vésicules séminales et des canaux déférents

Kassogué, Amadou, El Ammari, J. Eddine, Diarra, Alkadri, Amiroune, Driss, Ahsaini, Mustapha, Ouldim, Karim, Traoré, Zacharia, Sqalli, H. Nadia, Tizniti, Siham, Mellas, Soufiane, Tazi, M. Fadl, Khallou

Journal:

Canadian Urological Association Journal

Year:

2014

Language:

french

File:

PDF, 129 KB

french, 2014

27

GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot

EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Bouguenouch, Laila, Samri, Imane, Bouhrim, Mohamed, Ouldim, Karim, Atmani, Samir

Journal:

African Health Sciences

Year:

2018

Language:

english

File:

PDF, 371 KB

english, 2018

28

Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients

Hamdaoui, Hasna, Benlarroubia, Oumaima, Ait Boujmia, Oum Kaltoum, Mossafa, Hossein, Ouldim, Karim, Belkhayat, Aziza, Smyej, Imane, Benrahma, Houda, Dehbi, Hind, Chegdani, Fatima

Journal:

Molecular Genetics & Genomic Medicine

Year:

2020

File:

PDF, 987 KB

2020

29

Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review

El Asri, Achraf, Zarrouq, Btissame, El Kinany, Khaoula, Bouguenouch, Laila, Ouldim, Karim, El Rhazi, Karima

Journal:

Year:

2020

File:

PDF, 716 KB

2020

30

Cancer Omics in Africa: Present and Prospects

El Jaddaoui, Islam, Allali, Imane, Sehli, Sofia, Ouldim, Karim, Hamdi, Salsabil, Al Idrissi, Najib, Nejjari, Chakib, Amzazi, SaaÃ¯d, Bakri, Youssef, Ghazal, Hassan

Journal:

Frontiers in Oncology

Year:

2020

File:

PDF, 372 KB

2020

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