-
1
-
-
49449090548
-
-
National Statistics Institute of Tunisia
-
National Statistics Institute of Tunisia. www. ins.nat.tn/.
-
-
-
-
3
-
-
49449106196
-
-
online.fr
-
http://www.tunisie.online.fr.
-
-
-
-
4
-
-
49449092526
-
-
Ministry of Health Tunisia
-
Ministry of Health Tunisia. http://www.ministeres. tn/html/ministeres/ sante.html.
-
-
-
-
5
-
-
49449089027
-
-
http://www.santetunisie.rns.tn/msp/msp. html.
-
-
-
-
6
-
-
49449119008
-
-
Brace RM: Morocco, Algeria, Tunisia. Englewood Cliffs, Prentice-Hall, 1964, pp 39-52, 95-97.
-
Brace RM: Morocco, Algeria, Tunisia. Englewood Cliffs, Prentice-Hall, 1964, pp 39-52, 95-97.
-
-
-
-
7
-
-
49449084549
-
Histoire générale de la Tunisie des temps modernes (General history of modern Tunisia)
-
Slim H, Mahjoubi A, Belkhoja K, Ennabli A eds
-
Slim H, Mahjoubi A, Belkhoja K, Ennabli A (eds): Histoire générale de la Tunisie des temps modernes (General history of modern Tunisia). Arles, SUD, 2007.
-
(2007)
Arles, SUD
-
-
-
8
-
-
0024624615
-
Consanguinité dans la population du nord de la Tunisie
-
in French
-
Riou S, El Younsi C, Chaabouni H: Consanguinité dans la population du nord de la Tunisie (in French). Tunis Med 1989;67:167-172.
-
(1989)
Tunis Med
, vol.67
, pp. 167-172
-
-
Riou, S.1
El Younsi, C.2
Chaabouni, H.3
-
9
-
-
33747854482
-
Association among education level, occupation status, and consanguinity in Tunisia and Croatia
-
Kerkeni E, Monastiri K, Saket B, Rudan D, Zgaga L, Ben Cheikh H: Association among education level, occupation status, and consanguinity in Tunisia and Croatia. Croat Med J 2006;47:656-661.
-
(2006)
Croat Med J
, vol.47
, pp. 656-661
-
-
Kerkeni, E.1
Monastiri, K.2
Saket, B.3
Rudan, D.4
Zgaga, L.5
Ben Cheikh, H.6
-
10
-
-
49449109140
-
-
Alwan A, Modell B: Community control of genetic and congenital disorders. EMRO Technical Publication Series 24. Geneva, WHO Regional Office for the Eastern Mediterranean Region, 1997.
-
Alwan A, Modell B: Community control of genetic and congenital disorders. EMRO Technical Publication Series 24. Geneva, WHO Regional Office for the Eastern Mediterranean Region, 1997.
-
-
-
-
11
-
-
0026907457
-
Prevalence of hemoglobinopathies in Nefza: Study of 1303 patients
-
in French
-
Znaidi R, Hafsia R, M'Rad A, Belhadj A, Kastally R, Hafsia A: Prevalence of hemoglobinopathies in Nefza: study of 1303 patients (in French). Tunis Med 1992;70:400-404.
-
(1992)
Tunis Med
, vol.70
, pp. 400-404
-
-
Znaidi, R.1
Hafsia, R.2
M'Rad, A.3
Belhadj, A.4
Kastally, R.5
Hafsia, A.6
-
12
-
-
0032916851
-
Prevalence of hemoglobin abnormalities in Kebili (Tunisian South)
-
in French
-
Mseddi S, Gargouri J, Labiadh Z, Kassis M, Elloumi M, Ghali L, Dammak J, Harrabi M, Souissi T, Frikha M: Prevalence of hemoglobin abnormalities in Kebili (Tunisian South) (in French). Rev Epidemiol Sante Publique 1999;47:29-36.
-
(1999)
Rev Epidemiol Sante Publique
, vol.47
, pp. 29-36
-
-
Mseddi, S.1
Gargouri, J.2
Labiadh, Z.3
Kassis, M.4
Elloumi, M.5
Ghali, L.6
Dammak, J.7
Harrabi, M.8
Souissi, T.9
Frikha, M.10
-
13
-
-
33846139589
-
Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data
-
in French
-
Fattoum S: Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data (in French). Tunis Med 2006;84:687-696.
-
(2006)
Tunis Med
, vol.84
, pp. 687-696
-
-
Fattoum, S.1
-
14
-
-
4544319099
-
Molecular basis of beta-thalassemia in the population of Tunisia
-
Fattoum S, Messaoud T, Bibi A: Molecular basis of beta-thalassemia in the population of Tunisia. Hemoglobin 2004;28:177-187.
-
(2004)
Hemoglobin
, vol.28
, pp. 177-187
-
-
Fattoum, S.1
Messaoud, T.2
Bibi, A.3
-
15
-
-
4544255724
-
Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity
-
Chouk I, Daoud BB, Mellouli F, Bejaoui M, Gérard N, Dellagi K, Abbes S: Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity. Hemoglobin 2004;28:189-195.
-
(2004)
Hemoglobin
, vol.28
, pp. 189-195
-
-
Chouk, I.1
Daoud, B.B.2
Mellouli, F.3
Bejaoui, M.4
Gérard, N.5
Dellagi, K.6
Abbes, S.7
-
16
-
-
0033846618
-
Molecular analysis and prenatal diagnosis of beta-thalassemia: About our experience in central Tunisia
-
in French
-
Laradi S, Haj Khelil A, Omri H, Chaieb A, Mahjoub T, Benlimam H, Amri F, Saad A, Miled A, Leturcq F, Ben Chibani J, Beldjord C: Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia (in French). Ann Biol Clin (Paris) 2000;58:453-460.
-
(2000)
Ann Biol Clin (Paris)
, vol.58
, pp. 453-460
-
-
Laradi, S.1
Haj Khelil, A.2
Omri, H.3
Chaieb, A.4
Mahjoub, T.5
Benlimam, H.6
Amri, F.7
Saad, A.8
Miled, A.9
Leturcq, F.10
Ben Chibani, J.11
Beldjord, C.12
-
17
-
-
1842867709
-
Molecular spectrum of alpha-thalassemia in Tunisia: Epidemiology and detection at birth
-
Zorai A, Harteveld CL, Bakir A, Van Delft P, Falfoul A, Dellagi K, Abbes S, Giordano PC: Molecular spectrum of alpha-thalassemia in Tunisia: epidemiology and detection at birth. Hemoglobin 2002;26:353-362.
-
(2002)
Hemoglobin
, vol.26
, pp. 353-362
-
-
Zorai, A.1
Harteveld, C.L.2
Bakir, A.3
Van Delft, P.4
Falfoul, A.5
Dellagi, K.6
Abbes, S.7
Giordano, P.C.8
-
18
-
-
0041971230
-
Fanconi anemia in Tunisia: High prevalence of group A and identification of new FANCA mutations
-
Bouchlaka C, Abdelhak S, Amouri A, Ben Abid H, Hadiji S, Frikha M, Ben Othman T, Amri F, Ayadi H, Hachicha M, Rebaï A, Saad A, Dellagi K: Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. J Hum Genet 2003;48:352-361.
-
(2003)
J Hum Genet
, vol.48
, pp. 352-361
-
-
Bouchlaka, C.1
Abdelhak, S.2
Amouri, A.3
Ben Abid, H.4
Hadiji, S.5
Frikha, M.6
Ben Othman, T.7
Amri, F.8
Ayadi, H.9
Hachicha, M.10
Rebaï, A.11
Saad, A.12
Dellagi, K.13
-
19
-
-
16944365196
-
-
A candidate gene for familial Mediterranean fever. The French FMF Consortium. Nat Genet 1997;17:25-31.
-
A candidate gene for familial Mediterranean fever. The French FMF Consortium. Nat Genet 1997;17:25-31.
-
-
-
-
20
-
-
34248647027
-
MEFV mutations in Tunisian patients suffering from familial Mediterranean fever
-
Chaabouni Bouhamed H, Ksantini M, M'rad R, Kharrat M, Chaabouni M, Maazoul F, Bahloul Z, Ben Jemaa L, Ben Moussa F, Ben Chaabane T, Mrad S, Touitou I, Smaoui N: MEFV mutations in Tunisian patients suffering from familial Mediterranean fever. Semin Arthritis Rheum 2007;36:397-401.
-
(2007)
Semin Arthritis Rheum
, vol.36
, pp. 397-401
-
-
Chaabouni Bouhamed, H.1
Ksantini, M.2
M'rad, R.3
Kharrat, M.4
Chaabouni, M.5
Maazoul, F.6
Bahloul, Z.7
Ben Jemaa, L.8
Ben Moussa, F.9
Ben Chaabane, T.10
Mrad, S.11
Touitou, I.12
Smaoui, N.13
-
21
-
-
0842269752
-
Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: Identification of four novel mutations and high prevalence of Q318X mutation
-
Kharrat M, Tardy V, M'Rad R, Maazoul F, Jemaa LB, Refai M, Morel Y, Chaabouni H: Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation. J Clin Endocrinol Metab 2004;89:368-374.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 368-374
-
-
Kharrat, M.1
Tardy, V.2
M'Rad, R.3
Maazoul, F.4
Jemaa, L.B.5
Refai, M.6
Morel, Y.7
Chaabouni, H.8
-
22
-
-
28444443000
-
A novel 13-pb deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasia
-
Kharrat M, Tardy V, M'rad R, Maazoul F, Morel Y, Chaabouni H: A novel 13-pb deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasia. Diagn Mol Pathol 2005;14:250-252.
-
(2005)
Diagn Mol Pathol
, vol.14
, pp. 250-252
-
-
Kharrat, M.1
Tardy, V.2
M'rad, R.3
Maazoul, F.4
Morel, Y.5
Chaabouni, H.6
-
23
-
-
49449104817
-
11β-hydroxylase deficiency in Tunisia only due to two mutations of the CYP11B1 gene: G295V a novel mutation and Q356X
-
Chaabouni H, Menassa R, Maazoul F, Ftouhi B, Kamoun M, Kacem M, Jemaa LB, Morel Y: 11β-hydroxylase deficiency in Tunisia only due to two mutations of the CYP11B1 gene: G295V a novel mutation and Q356X. Horm Res 2005;64(suppl 1):336-337.
-
(2005)
Horm Res
, vol.64
, Issue.SUPPL. 1
, pp. 336-337
-
-
Chaabouni, H.1
Menassa, R.2
Maazoul, F.3
Ftouhi, B.4
Kamoun, M.5
Kacem, M.6
Jemaa, L.B.7
Morel, Y.8
-
24
-
-
0029931804
-
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: Identification of two novel mutations
-
Messaoud T, Verlingue C, Denamur E, Pascaud O, Quere I, Fattoum S, Elion J, Ferec C: Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations. Eur J Hum Genet 1996;4:20-24.
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 20-24
-
-
Messaoud, T.1
Verlingue, C.2
Denamur, E.3
Pascaud, O.4
Quere, I.5
Fattoum, S.6
Elion, J.7
Ferec, C.8
-
25
-
-
29544437152
-
Molecular epidemiology of cystic fibrosis in Tunisia
-
in French
-
Messaoud T, Bel Haj Fredj S, Bibi A, Elion J, Ferec C, Fattoum S: Molecular epidemiology of cystic fibrosis in Tunisia (in French). Ann Biol Clin (Paris) 2005;63:627-630.
-
(2005)
Ann Biol Clin (Paris)
, vol.63
, pp. 627-630
-
-
Messaoud, T.1
Bel2
Haj Fredj, S.3
Bibi, A.4
Elion, J.5
Ferec, C.6
Fattoum, S.7
-
26
-
-
0022762661
-
Etude génétique des hérédodégénérescences spino- cérébelleuses: Le rôle de la consanguinité dans leur survenue
-
in French
-
Ben Hamida M, Chaabouni H, Madani S, Boussen S, Sammoud S, Letaief F, Mrabet A, Hentati F, Miladi N: Etude génétique des hérédodégénérescences spino- cérébelleuses: le rôle de la consanguinité dans leur survenue (in French). J Génét Hum 1986;34:267-275.
-
(1986)
J Génét Hum
, vol.34
, pp. 267-275
-
-
Ben Hamida, M.1
Chaabouni, H.2
Madani, S.3
Boussen, S.4
Sammoud, S.5
Letaief, F.6
Mrabet, A.7
Hentati, F.8
Miladi, N.9
-
27
-
-
33845361572
-
Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients
-
Mrad R, Dorboz I, Ben Jemaa L, Maazoul F, Trabelsi M, Chaabouni M, Mlaiki B, Miladi N, Hentati F, Chaabouni H: Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients. Tunis Med 2006;84:465-469.
-
(2006)
Tunis Med
, vol.84
, pp. 465-469
-
-
Mrad, R.1
Dorboz, I.2
Ben Jemaa, L.3
Maazoul, F.4
Trabelsi, M.5
Chaabouni, M.6
Mlaiki, B.7
Miladi, N.8
Hentati, F.9
Chaabouni, H.10
-
28
-
-
0020554622
-
Autosomal recessive severe, proximal myopathy in children, common in Tunisia
-
in French
-
Ben Hamida M, Attia N, Chabouni H, Fardeau M: Autosomal recessive severe, proximal myopathy in children, common in Tunisia (in French). Rev Neurol (Paris) 1983;139:289-297.
-
(1983)
Rev Neurol (Paris)
, vol.139
, pp. 289-297
-
-
Ben Hamida, M.1
Attia, N.2
Chabouni, H.3
Fardeau, M.4
-
29
-
-
0027032694
-
Linkage of Tunisian autosomal recessive Duchennelike muscular dystrophy to the pericentromeric region of chromosome 13q
-
Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, Hentati F, Vance JM: Linkage of Tunisian autosomal recessive Duchennelike muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet 1992;2:315-317.
-
(1992)
Nat Genet
, vol.2
, pp. 315-317
-
-
Ben Othmane, K.1
Ben Hamida, M.2
Pericak-Vance, M.A.3
Ben Hamida, C.4
Blel, S.5
Carter, S.C.6
Bowcock, A.M.7
Petruhkin, K.8
Gilliam, T.C.9
Roses, A.D.10
Hentati, F.11
Vance, J.M.12
-
30
-
-
0027514838
-
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
-
Ben Hamida C, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D: Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat Genet 1993;5:195-200.
-
(1993)
Nat Genet
, vol.5
, pp. 195-200
-
-
Ben Hamida, C.1
Doerflinger, N.2
Belal, S.3
Linder, C.4
Reutenauer, L.5
Dib, C.6
Gyapay, G.7
Vignal, A.8
Le Paslier, D.9
Cohen, D.10
-
31
-
-
0028334717
-
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35
-
Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C: Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Nat Genet 1994;7:425-428.
-
(1994)
Nat Genet
, vol.7
, pp. 425-428
-
-
Hentati, A.1
Bejaoui, K.2
Pericak-Vance, M.A.3
Hentati, F.4
Speer, M.C.5
Hung, W.Y.6
Figlewicz, D.A.7
Haines, J.8
Rimmler, J.9
Ben Hamida, C.10
-
32
-
-
0031215451
-
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
-
Ben Hamida C, Cavalier L, Belal S, Sanhaji H, Nadal N, Barhoumi C, M'Rissa N, Marzouki N, Mandel JL, Ben Hamida M, Koenig M, Hentati F: Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1. Neurogenetics 1997;1:129-133.
-
(1997)
Neurogenetics
, vol.1
, pp. 129-133
-
-
Ben Hamida, C.1
Cavalier, L.2
Belal, S.3
Sanhaji, H.4
Nadal, N.5
Barhoumi, C.6
M'Rissa, N.7
Marzouki, N.8
Mandel, J.L.9
Ben Hamida, M.10
Koenig, M.11
Hentati, F.12
-
33
-
-
17344376225
-
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15
-
Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM: Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics 1999;62:344-349.
-
(1999)
Genomics
, vol.62
, pp. 344-349
-
-
Othmane, K.B.1
Johnson, E.2
Menold, M.3
Graham, F.L.4
Hamida, M.B.5
Hasegawa, O.6
Rogala, A.D.7
Ohnishi, A.8
Pericak-Vance, M.9
Hentati, F.10
Vance, J.M.11
-
34
-
-
0034214277
-
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
-
Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F: A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. Neuromuscul Disord 2000;10:240-246.
-
(2000)
Neuromuscul Disord
, vol.10
, pp. 240-246
-
-
Driss, A.1
Amouri, R.2
Ben Hamida, C.3
Souilem, S.4
Gouider-Khouja, N.5
Ben Hamida, M.6
Hentati, F.7
-
35
-
-
0034636165
-
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
-
Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F: Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology 2000;54:1408-1414.
-
(2000)
Neurology
, vol.54
, pp. 1408-1414
-
-
Mrissa, N.1
Belal, S.2
Hamida, C.B.3
Amouri, R.4
Turki, I.5
Mrissa, R.6
Hamida, M.B.7
Hentati, F.8
-
36
-
-
0035144845
-
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3
-
Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F: Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. Neuromuscul Disord 2001;11:27-34.
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 27-34
-
-
Barhoumi, C.1
Amouri, R.2
Ben Hamida, C.3
Ben Hamida, M.4
Machghoul, S.5
Gueddiche, M.6
Hentati, F.7
-
37
-
-
0038699003
-
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
-
Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F: Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism Relat Disord 2003;9:247-251.
-
(2003)
Parkinsonism Relat Disord
, vol.9
, pp. 247-251
-
-
Gouider-Khouja, N.1
Larnaout, A.2
Amouri, R.3
Sfar, S.4
Belal, S.5
Ben Hamida, C.6
Ben Hamida, M.7
Hattori, N.8
Mizuno, Y.9
Hentati, F.10
-
38
-
-
0035319979
-
Melanoma in xeroderma pigmentosum: 12 cases
-
in French
-
Fazaa B, Zghal M, Bailly C, Zeglaoui F, Goucha S, Mokhtar I, Kharfi M, Ezzine N, Kamoun MR: Melanoma in xeroderma pigmentosum: 12 cases (in French). Ann Dermatol Venereol 2001;128:503-506.
-
(2001)
Ann Dermatol Venereol
, vol.128
, pp. 503-506
-
-
Fazaa, B.1
Zghal, M.2
Bailly, C.3
Zeglaoui, F.4
Goucha, S.5
Mokhtar, I.6
Kharfi, M.7
Ezzine, N.8
Kamoun, M.R.9
-
39
-
-
30544440179
-
-
Zghal M, El-Fekih N, Fazaa B, Fredj M, Zhioua R, Mokhtar I, Mrabet A, Ferjani M, Gaigi S, Kamoun MR: Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 49 Tunisian cases (in French). Tunis Med 2005;83:760-763.
-
Zghal M, El-Fekih N, Fazaa B, Fredj M, Zhioua R, Mokhtar I, Mrabet A, Ferjani M, Gaigi S, Kamoun MR: Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 49 Tunisian cases (in French). Tunis Med 2005;83:760-763.
-
-
-
-
40
-
-
0027359248
-
High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia
-
Nishigori C, Zghal M, Yagi T, Imamura S, Komoun MR, Takebe H: High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia. Am J Hum Genet 1993;53:1001-1006.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1001-1006
-
-
Nishigori, C.1
Zghal, M.2
Yagi, T.3
Imamura, S.4
Komoun, M.R.5
Takebe, H.6
-
41
-
-
49449094218
-
Hereditary epidermolysis bullosa in Tunisia: An epidemio-clinical and ultrastructural study
-
in French
-
Cherif F, Mnajja N, Feriani S, Ben Saïd ZM, Jaafoura MH, Dhahri AB, Boubaker S: Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study (in French). Tunis Med 2005;83:760-763.
-
(2005)
Tunis Med
, vol.83
, pp. 760-763
-
-
Cherif, F.1
Mnajja, N.2
Feriani, S.3
Ben Saïd, Z.M.4
Jaafoura, M.H.5
Dhahri, A.B.6
Boubaker, S.7
-
42
-
-
35448962049
-
A study of skin diseases in Tunis. An analysis of 28,244 dermatological outpatient cases
-
Souissi A, Zeglaoui F, Zouari B, Kamoun MR: A study of skin diseases in Tunis. An analysis of 28,244 dermatological outpatient cases. Acta Dermatovenerol Alp Panonica Adriat 2007;16:111-116.
-
(2007)
Acta Dermatovenerol Alp Panonica Adriat
, vol.16
, pp. 111-116
-
-
Souissi, A.1
Zeglaoui, F.2
Zouari, B.3
Kamoun, M.R.4
-
43
-
-
33749061661
-
Hereditary epidermolysis bullosa in Tunisia: An epidemio-clinical and ultrastructural study
-
in French
-
Cherif F, Mnajja N, Feriani S, Ben Saïd ZM, Jaafoura MH, Dhahri AB, Boubaker S: Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study (in French). Arch Inst Pasteur Tunis 2005;82:53-58.
-
(2005)
Arch Inst Pasteur Tunis
, vol.82
, pp. 53-58
-
-
Cherif, F.1
Mnajja, N.2
Feriani, S.3
Ben Saïd, Z.M.4
Jaafoura, M.H.5
Dhahri, A.B.6
Boubaker, S.7
-
44
-
-
49449112005
-
Les malformations congénitales: Dépistage néonatal dans une maternité tunisienne
-
in French
-
Chaabouni H, Nemsia J, Riou S, Largueche S, Ferchiou A: Les malformations congénitales: dépistage néonatal dans une maternité tunisienne (in French). Maghreb Med 1986;129:49-54.
-
(1986)
Maghreb Med
, vol.129
, pp. 49-54
-
-
Chaabouni, H.1
Nemsia, J.2
Riou, S.3
Largueche, S.4
Ferchiou, A.5
-
45
-
-
0022617635
-
Malformations in 10,000 consecutive births in Tunis
-
Khrouf N, Spång R, Podgorna T, Miled SB, Moussaoui M, Chibani M: Malformations in 10,000 consecutive births in Tunis. Acta Paediatr Scand 1986;75:534-539.
-
(1986)
Acta Paediatr Scand
, vol.75
, pp. 534-539
-
-
Khrouf, N.1
Spång, R.2
Podgorna, T.3
Miled, S.B.4
Moussaoui, M.5
Chibani, M.6
-
46
-
-
13244252565
-
Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family
-
Chaabouni M, Smaoui N, Benneji N, M'rad R, Jemaa LB, Hachicha S, Chaabouni H: Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family. Clin Dysmorphol 2005;14:23-25.
-
(2005)
Clin Dysmorphol
, vol.14
, pp. 23-25
-
-
Chaabouni, M.1
Smaoui, N.2
Benneji, N.3
M'rad, R.4
Jemaa, L.B.5
Hachicha, S.6
Chaabouni, H.7
-
47
-
-
0030896802
-
Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: Evidence for founder effect and genomic recombination at the CA II locus
-
Fathallah DM, Bejaoui M, Lepaslier D, Chater K, Sly WS, Dellagi K: Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locus. Hum Genet 1997;99:634-637.
-
(1997)
Hum Genet
, vol.99
, pp. 634-637
-
-
Fathallah, D.M.1
Bejaoui, M.2
Lepaslier, D.3
Chater, K.4
Sly, W.S.5
Dellagi, K.6
-
48
-
-
33748093622
-
Screening of the eight BBS genes in Tunisian families: No evidence of triallelism
-
Smaoui N, Chaabouni M, Sergeev YV, Kallel H, Li S, Mahfoudh N, Maazoul F, Kammoun H, Gandoura N, Bouaziz A, Nouiri E, M'Rad R, Chaabouni H, Hejtmancik JF: Screening of the eight BBS genes in Tunisian families: no evidence of triallelism. Invest Ophthalmol Vis Sci 2006;47:3487-3495.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 3487-3495
-
-
Smaoui, N.1
Chaabouni, M.2
Sergeev, Y.V.3
Kallel, H.4
Li, S.5
Mahfoudh, N.6
Maazoul, F.7
Kammoun, H.8
Gandoura, N.9
Bouaziz, A.10
Nouiri, E.11
M'Rad, R.12
Chaabouni, H.13
Hejtmancik, J.F.14
-
49
-
-
0028185868
-
Clinical aspects of Schwartz Jampel syndrome: 4 new familial case reports and review of the literature
-
in French
-
Karboul L, Samoud A, Hammou A, Ben Dridi MF: Clinical aspects of Schwartz Jampel syndrome: 4 new familial case reports and review of the literature (in French). Tunis Med 1994;72:39-45.
-
(1994)
Tunis Med
, vol.72
, pp. 39-45
-
-
Karboul, L.1
Samoud, A.2
Hammou, A.3
Ben Dridi, M.F.4
-
50
-
-
33846121329
-
Robinow syndrome: Report of two cases and review of the literature
-
Al Kaissi A, Biegansk T, Baranska D, Chehida FB, Gharbi H, Ghachem MB, Hendaoui L, Safi H, Kozlowski K: Robinow syndrome: report of two cases and review of the literature. Australas Radiol 2007;5:83-86.
-
(2007)
Australas Radiol
, vol.5
, pp. 83-86
-
-
Al Kaissi, A.1
Biegansk, T.2
Baranska, D.3
Chehida, F.B.4
Gharbi, H.5
Ghachem, M.B.6
Hendaoui, L.7
Safi, H.8
Kozlowski, K.9
-
51
-
-
0033870093
-
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome
-
Hadj-Rabia S, Salomon R, Pelet A, Penet C, Rotschild A, de Laet MH, Chaouachi B, Hannachi R, Bakiri F, Brauner R, Chaussain JL, Munnich A, Lyonnet S: Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome. Eur J Hum Genet 2000;8:613-620.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 613-620
-
-
Hadj-Rabia, S.1
Salomon, R.2
Pelet, A.3
Penet, C.4
Rotschild, A.5
de Laet, M.H.6
Chaouachi, B.7
Hannachi, R.8
Bakiri, F.9
Brauner, R.10
Chaussain, J.L.11
Munnich, A.12
Lyonnet, S.13
-
52
-
-
33846785380
-
-
Al Kaissi A, Klaushofer K, Safi H, Chehida FB, Ghachem MB, Chaabounni M, Hennekam RC: Asymmetrical skull, ptosis, hypertelorism, high nasal bridge, clefting, umbilical anomalies, and skeletal anomalies in sibs: is Carnevale syndrome a separate entity? Am J Med Genet A 2007;143:349-354.
-
(2007)
Asymmetrical skull, ptosis, hypertelorism, high nasal bridge, clefting, umbilical anomalies, and skeletal anomalies in sibs: Is Carnevale syndrome a separate entity? Am J Med Genet A
, vol.143
, pp. 349-354
-
-
Al Kaissi, A.1
Klaushofer, K.2
Safi, H.3
Chehida, F.B.4
Ghachem, M.B.5
Chaabounni, M.6
Hennekam, R.C.7
-
53
-
-
0026483579
-
Cytogenetic study of 500 patients selected in the research for chromosomal anomalies
-
in French
-
Chaabouni H, Meddeb M, Buresi C, Ben Jemaa L: Cytogenetic study of 500 patients selected in the research for chromosomal anomalies (in French). Tunis Med 1992;70:39-43.
-
(1992)
Tunis Med
, vol.70
, pp. 39-43
-
-
Chaabouni, H.1
Meddeb, M.2
Buresi, C.3
Ben Jemaa, L.4
-
54
-
-
33751167216
-
Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders
-
Elghezal H, Hidar S, Braham R, Denguezli W, Ajina M, Saad A: Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders. Fertil Steril 2006;86:1792-1795.
-
(2006)
Fertil Steril
, vol.86
, pp. 1792-1795
-
-
Elghezal, H.1
Hidar, S.2
Braham, R.3
Denguezli, W.4
Ajina, M.5
Saad, A.6
-
55
-
-
34248186060
-
De novo trisomy 20p of paternal origin
-
Chaabouni M, Turleau C, Karboul L, Jemaa LB, Maazoul F, Attié-Bitach H, Romana S, Chaabouni H: De novo trisomy 20p of paternal origin. Am J Med Genet A 2007;143:1100-1103.
-
(2007)
Am J Med Genet A
, vol.143
, pp. 1100-1103
-
-
Chaabouni, M.1
Turleau, C.2
Karboul, L.3
Jemaa, L.B.4
Maazoul, F.5
Attié-Bitach, H.6
Romana, S.7
Chaabouni, H.8
-
56
-
-
0033169729
-
Etude épidémiologique et génétique de la trisomie 21 en Tunisie
-
in French
-
Chaabouni H, Smaoui N, Maazoul F, Ben Jemaa L, M'Rad R: Etude épidémiologique et génétique de la trisomie 21 en Tunisie (in French). Tunis Med 1999;77:407-414.
-
(1999)
Tunis Med
, vol.77
, pp. 407-414
-
-
Chaabouni, H.1
Smaoui, N.2
Maazoul, F.3
Ben Jemaa, L.4
M'Rad, R.5
-
57
-
-
0025103230
-
An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul)
-
Ben Arab S, Bonaïti-Pellié C, Belkahia A: An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul). J Med Genet 1990;27:29-33.
-
(1990)
J Med Genet
, vol.27
, pp. 29-33
-
-
Ben Arab, S.1
Bonaïti-Pellié, C.2
Belkahia, A.3
-
58
-
-
3042520840
-
Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness
-
Ben Arab S, Masmoudi S, Beltaief N, Hachicha S, Ayadi H: Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness. Genet Epidemiol 2004;27:74-79.
-
(2004)
Genet Epidemiol
, vol.27
, pp. 74-79
-
-
Ben Arab, S.1
Masmoudi, S.2
Beltaief, N.3
Hachicha, S.4
Ayadi, H.5
-
59
-
-
0028249690
-
A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q
-
Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C: A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nat Genet 1994;6:24-28.
-
(1994)
Nat Genet
, vol.6
, pp. 24-28
-
-
Guilford, P.1
Ben Arab, S.2
Blanchard, S.3
Levilliers, J.4
Weissenbach, J.5
Belkahia, A.6
Petit, C.7
-
60
-
-
9844252338
-
Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene
-
Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn AH, Dahl HH, Middleton A, Houseman MJ, Dodé C, Marlin S, Boulila-ElGaïed A, Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha M, Loiselet J, El-Zir E, Aubois A, Joannard A, Petit C, et al: Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet 1997;6:2173-2177.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2173-2177
-
-
Denoyelle, F.1
Weil, D.2
Maw, M.A.3
Wilcox, S.A.4
Lench, N.J.5
Allen-Powell, D.R.6
Osborn, A.H.7
Dahl, H.H.8
Middleton, A.9
Houseman, M.J.10
Dodé, C.11
Marlin, S.12
Boulila-ElGaïed, A.13
Grati, M.14
Ayadi, H.15
BenArab, S.16
Bitoun, P.17
Lina-Granade, G.18
Godet, J.19
Mustapha, M.20
Loiselet, J.21
El-Zir, E.22
Aubois, A.23
Joannard, A.24
Petit, C.25
more..
-
61
-
-
31144451029
-
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family
-
Tilli A, Männikkö M, Charfedine I, Lahmar I, Benzina Z, Ben Amor M, Driss N, Ala-Kokko L, Drira M, Masmoudi S, Ayadi H: A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family. Hum Hered 2005;60:123-128.
-
(2005)
Hum Hered
, vol.60
, pp. 123-128
-
-
Tilli, A.1
Männikkö, M.2
Charfedine, I.3
Lahmar, I.4
Benzina, Z.5
Ben Amor, M.6
Driss, N.7
Ala-Kokko, L.8
Drira, M.9
Masmoudi, S.10
Ayadi, H.11
-
62
-
-
0037299314
-
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1
-
Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H: Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. Eur J Hum Genet 2003;11:185-188.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 185-188
-
-
Masmoudi, S.1
Tlili, A.2
Majava, M.3
Ghorbel, A.M.4
Chardenoux, S.5
Lemainque, A.6
Zina, Z.B.7
Moala, J.8
Männikkö, M.9
Weil, D.10
Lathrop, M.11
Ala-Kokko, L.12
Drira, M.13
Petit, C.14
Ayadi, H.15
-
63
-
-
0032958299
-
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2
-
Hmani M, Ghorbel A, Boulila-Elgaied A, Ben Zina Z, Kammoun W, Drira M, Chaabouni M, Petit C, Ayadi H: A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2. Eur J Hum Genet 1999;7:363-367.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 363-367
-
-
Hmani, M.1
Ghorbel, A.2
Boulila-Elgaied, A.3
Ben Zina, Z.4
Kammoun, W.5
Drira, M.6
Chaabouni, M.7
Petit, C.8
Ayadi, H.9
-
64
-
-
0033987133
-
Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation
-
Masmoudi S, Charfedine I, Hmani M, Grati M, Ghorbel AM, Elgaied-Boulila A, Drira M, Hardelin JP, Ayadi H: Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation. Am J Med Genet 2000;90:38-44.
-
(2000)
Am J Med Genet
, vol.90
, pp. 38-44
-
-
Masmoudi, S.1
Charfedine, I.2
Hmani, M.3
Grati, M.4
Ghorbel, A.M.5
Elgaied-Boulila, A.6
Drira, M.7
Hardelin, J.P.8
Ayadi, H.9
-
65
-
-
3242880191
-
A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract
-
Smaoui N, Beltaief O, Ben Hamed S, M'Rad R, Maazoul F, Ouertani A, Chaabouni H, Hejtmancik JF: A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract. Invest Ophthalmol Vis Sci 2004;45:2716-2721.
-
(2004)
Invest Ophthalmol Vis Sci
, vol.45
, pp. 2716-2721
-
-
Smaoui, N.1
Beltaief, O.2
Ben Hamed, S.3
M'Rad, R.4
Maazoul, F.5
Ouertani, A.6
Chaabouni, H.7
Hejtmancik, J.F.8
-
66
-
-
49449095559
-
-
www.iph.nat.tn.
-
-
-
-
67
-
-
0033036626
-
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)
-
Jemaa LB, des Portes V, Zemni R, Mrad R, Maazoul F, Beldjord C, Chaabouni H, Chelly J: Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54). Am J Med Genet 1999;85:276-282.
-
(1999)
Am J Med Genet
, vol.85
, pp. 276-282
-
-
Jemaa, L.B.1
des Portes, V.2
Zemni, R.3
Mrad, R.4
Maazoul, F.5
Beldjord, C.6
Chaabouni, H.7
Chelly, J.8
-
68
-
-
0037090887
-
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
-
Bienvenu T, Poirier K, Friocourt G, Bahi N, Beaumont D, Fauchereau F, Benjemaa L, Zemni R, Vinet MC, Francis F, Couvert P, Gomot M, Moraine C, Van Bokhoven H, Kalscheuer V, Frints S, Gecz J, Ohzaki K, Chaabouni H, Desportes V, Fryns JP, Beldjord C, Chelly J: ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation. Hum Mol Genet 2002;11:981-991.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 981-991
-
-
Bienvenu, T.1
Poirier, K.2
Friocourt, G.3
Bahi, N.4
Beaumont, D.5
Fauchereau, F.6
Benjemaa, L.7
Zemni, R.8
Vinet, M.C.9
Francis, F.10
Couvert, P.11
Gomot, M.12
Moraine, C.13
Van Bokhoven, H.14
Kalscheuer, V.15
Frints, S.16
Gecz, J.17
Ohzaki, K.18
Chaabouni, H.19
Desportes, V.20
Fryns, J.P.21
Beldjord, C.22
Chelly, J.23
more..
-
69
-
-
49449118071
-
Les sphingolipidoses chez l'enfant: À propos de 18 observations
-
in French
-
Trabelsi M, Elhammami A, Toumi N, Bousnina S, Boudhina T, Chaabouni H, Bennaceur B: Les sphingolipidoses chez l'enfant: à propos de 18 observations (in French). Tunis Med 1990;8:520-524.
-
(1990)
Tunis Med
, vol.8
, pp. 520-524
-
-
Trabelsi, M.1
Elhammami, A.2
Toumi, N.3
Bousnina, S.4
Boudhina, T.5
Chaabouni, H.6
Bennaceur, B.7
-
70
-
-
9144245510
-
La maladie de Gaucher en Tunisie, étude multicentrique
-
in French
-
Chaabouni M, Aoulou H, Tebib N, Hachicha M, Ben Becher S, Monastiri K, Yacoub M, Sfar T, Elloumi M, Chakroun N, Miled M, Ben Dridi MF: La maladie de Gaucher en Tunisie, étude multicentrique (in French). Rev Med Interne 2004;25:104-110.
-
(2004)
Rev Med Interne
, vol.25
, pp. 104-110
-
-
Chaabouni, M.1
Aoulou, H.2
Tebib, N.3
Hachicha, M.4
Ben Becher, S.5
Monastiri, K.6
Yacoub, M.7
Sfar, T.8
Elloumi, M.9
Chakroun, N.10
Miled, M.11
Ben Dridi, M.F.12
-
71
-
-
0034850494
-
Prenatal diagnosis of chromosome disorders in Tunisian population
-
Chaabouni H, Chaabouni M, Maazoul F, M'Rad R, Jemaa LB, Smaoui N, Terras K, Kammoun H, Belghith N, Ridene H, Oueslati B, Zouari F: Prenatal diagnosis of chromosome disorders in Tunisian population. Ann Genet 2001;44:99-104.
-
(2001)
Ann Genet
, vol.44
, pp. 99-104
-
-
Chaabouni, H.1
Chaabouni, M.2
Maazoul, F.3
M'Rad, R.4
Jemaa, L.B.5
Smaoui, N.6
Terras, K.7
Kammoun, H.8
Belghith, N.9
Ridene, H.10
Oueslati, B.11
Zouari, F.12
|