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| Title : Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene - Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
| Author(s) : Louhichi N , Bahloul E , Marrakchi S , Othman HB , Triki C , Aloulou K , Trabelsi L , Mahfouth N , Ayadi-Mnif Z , Keskes L , Fakhfakh F , Turki H |
| Ref : Orphanet J Rare Dis , 14 :112 , 2019 |
| Abstract : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
| ESTHER : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
| PubMedSearch : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
| PubMedID: 31118107 |
| Gene_locus related to this paper: human-ABHD5 |
| Title : [Myasthenia gravis and hyperthyroidism: two cases] - Trabelsi_2006_Ann.Endocrinol.(Paris)_67_265 |
| Author(s) : Trabelsi L , Charfi N , Triki C , Mnif M , Rekik N , Mhiri C , Abid M |
| Ref : Ann Endocrinol (Paris) , 67 :265 , 2006 |
| Abstract : Trabelsi_2006_Ann.Endocrinol.(Paris)_67_265 |
| ESTHER : Trabelsi_2006_Ann.Endocrinol.(Paris)_67_265 |
| PubMedSearch : Trabelsi_2006_Ann.Endocrinol.(Paris)_67_265 |
| PubMedID: 16840920 |