Mukaddam, Mona Al
23  Ergebnisse:
Personensuche X
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1

Garetosmab in fibrodysplasia ossificans progressiva:a rando..:

di Rocco, Maja ; Forleo-Neto, Eduardo ; Pignolo, Robert J...
https://research.vumc.nl/en/publications/17c58423-416d-4035-93e4-5aa4b74c387b.  , 2023
 
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3

Reduction of new heterotopic ossification (HO) in the open-..:

Pignolo, Robert J ; Hsiao, Edward C ; Al Mukaddam, Mona...
Journal of Bone and Mineral Research, 0884-0431, 2023, 38:3, s. 381-394.  , 2023
 
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4

Garetosmab in fibrodysplasia ossificans progressiva:a rando..:

di Rocco, Maja ; Forleo-Neto, Eduardo ; Pignolo, Robert J...
https://research.vumc.nl/en/publications/17c58423-416d-4035-93e4-5aa4b74c387b.  , 2023
 
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5

The natural history of fibrodysplasia ossificans progressiv..:

Pignolo, Robert J ; Baujat, Geneviève ; Brown, Matthew A...
https://kclpure.kcl.ac.uk/portal/en/publications/c00666b6-c4b9-4d66-9aed-a8c2aa608ddb.  , 2022
 
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6

Patients with ACVR1 R206H mutations have an increased preva..:

Kou, Samuel ; De Cunto, Carmen ; Baujat, Geneviève...
Kou , S , De Cunto , C , Baujat , G , Wentworth , K L , Grogan , D R , Brown , M A , Di Rocco , M , Keen , R , Al Mukaddam , M , le Quan Sang , K H , Masharani , U , Kaplan , F S , Pignolo , R J & Hsiao , E C 2020 , ' Patients with ACVR1 R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva ' , Orphanet Journal of Rare Diseases , vol. 15 , no. 1 , 193 . https://doi.org/10.1186/s13023-020-01465-x.  , 2020
 
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7

Patients with ACVR1 R206H mutations have an increased preva..:

Kou, Samuel ; De Cunto, Carmen ; Baujat, Geneviève...
Kou , S , De Cunto , C , Baujat , G , Wentworth , K L , Grogan , D R , Brown , M A , Di Rocco , M , Keen , R , Al Mukaddam , M , le Quan Sang , K H , Masharani , U , Kaplan , F S , Pignolo , R J & Hsiao , E C 2020 , ' Patients with ACVR1 R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva ' , Orphanet Journal of Rare Diseases , vol. 15 , no. 1 , 193 . https://doi.org/10.1186/s13023-020-01465-x.  , 2020
 
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9

Special considerations for clinical trials in fibrodysplasi..:

Hsiao, Edward C ; di Rocco, Maja ; Cali, Amanda...
https://research.vumc.nl/en/publications/c8d159b4-4870-4034-be34-f3724d9c5f63.  , 2019
 
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14

Natural history of fibrodysplasia ossificans progressiva:Cr..:

Pignolo, Robert J ; Baujat, Geneviève ; Brown, Matthew A...
Pignolo , R J , Baujat , G , Brown , M A , De Cunto , C , Dirocco , M , Hsiao , E C , Keen , R , Al Mukaddam , M , Sang , K H L Q , Wilson , A , White , B , Grogan , D R & Kaplan , F S 2019 , ' Natural history of fibrodysplasia ossificans progressiva : Cross-sectional analysis of annotated baseline phenotypes ' , Orphanet Journal of Rare Diseases , vol. 14 , no. 1 , 98 , pp. 1-11 . https://doi.org/10.1186/s13023-019-1068-7.  , 2019
 
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15

Natural history of fibrodysplasia ossificans progressiva:Cr..:

Pignolo, Robert J ; Baujat, Geneviève ; Brown, Matthew A...
Pignolo , R J , Baujat , G , Brown , M A , De Cunto , C , Dirocco , M , Hsiao , E C , Keen , R , Al Mukaddam , M , Sang , K H L Q , Wilson , A , White , B , Grogan , D R & Kaplan , F S 2019 , ' Natural history of fibrodysplasia ossificans progressiva : Cross-sectional analysis of annotated baseline phenotypes ' , Orphanet Journal of Rare Diseases , vol. 14 , no. 1 , 98 , pp. 1-11 . https://doi.org/10.1186/s13023-019-1068-7.  , 2019
 
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