|
🐜
|
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
38 auth.
A. Nicholas,
E. Serra,
H. Cangul,
S. Alyaarubi,
I. Ullah,
E. Schoenmakers,
A. Deeb,
A. Habeb,
Mohammad S. Al-Maghamsi,
C. Peters,
N. Nathwani,
Z. Aycan,
H. Sağlam,
Ece Böber,
M. Dattani,
...
Savitha D Shenoy,
P. Murray,
A. Babiker,
R. Willemsen,
A. Thankamony,
G. Lyons,
R. Irwin,
Raja Padidela,
Raja Padidela,
K. Tharian,
J. Davies,
Vijith R Puthi,
Soo-Mi Park,
A. Massoud,
J. Gregory,
A. Albanese,
Evelien Pease-Gevers,
H. Martin,
Kim Brügger,
E. Maher,
V. Chatterjee,
C. Anderson,
N. Schoenmakers
|
6 |
2016 |
6
🐜
|
|
🐜
|
Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes
17 auth.
Matthew B. Johnson,
E. De Franco,
Hana Lango Allen,
Aisha Al Senani,
N. Elbarbary,
Z. Şıklar,
M. Berberoğlu,
Z. Imane,
A. Haghighi,
Z. Razavi,
...
Irfan Ullah,
S. Alyaarubi,
D. Gardner,
Ayla Güven,
S. Ellard,
A. Hattersley,
S. Flanagan
|
5 |
2017 |
5
🐜
|
|
🐜
|
Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study
35 auth.
V. De Sanctis,
D. Canatan,
J. L. Corrons,
M. Karimi,
S. Daar,
C. Kattamis,
A. Soliman,
Y. Wali,
S. Alkindi,
V. Huseynov,
Afag Nasibova,
T. Tiryaki,
M. Evim,
A. Gunes,
Z. Karakaş,
...
S. Christou,
S. Campisi,
T. Zarei,
Doaa Khater,
Y. Oymak,
V. Kaleva,
D. Stoyanova,
A. Banchev,
M. Galati,
M. Yassin,
S. Kakar,
M. Skafida,
Y. Kilinç,
S. Alyaarubi,
Narmin Verdiyevas,
I. Stoeva,
G. Raiola,
D. Mariannis,
L. Ruggiero,
S. Di Maio
|
5 |
2020 |
5
🐜
|
|
🦁
|
Diabetes Care in Oman Obstacles and solutions
S. Alyaarubi
|
4 |
2011 |
4
🦁
|
|
🐜
|
An ICET-A survey on occult and emerging endocrine complications in patients with β-thalassemia major: Conclusions and recommendations
31 auth.
V. De Sanctis,
A. Soliman,
D. Canatan,
Ploutarchos Tzoulis,
S. Daar,
S. Di Maio,
H. Elsedfy,
M. Yassin,
A. Filosa,
N. Soliman,
K. Mehran,
F. Saki,
P. Sobti,
S. Kakkar,
S. Christou,
...
A. Albu,
C. Christodoulides,
Y. Kilinç,
Soad Al Jaouni,
Doaa Khater,
S. Alyaarubi,
S. Lum,
S. Campisi,
S. Anastasi,
M. Galati,
G. Raiola,
Y. Wali,
I. Elhakim,
D. Mariannis,
V. Ladis,
C. Kattamis
|
4 |
2019 |
4
🐜
|
|
🐬
|
Primary Hyperparathyroidism Mimicking Vaso-occlusive Crises in Sickle Cell Disease
Preetha Krishnamoorthy,
S. Alyaarubi,
S. Abish,
M. Gale,
P. Albuquerque,
N. Jabado
|
3 |
2006 |
3
🐬
|
|
🐜
|
Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study
26 auth.
M. Karimi,
T. Zarei,
S. Haghpanah,
A. Azarkeivan,
C. Kattamis,
V. Ladis,
A. Kattamis,
Y. Kilinç,
S. Daar,
S. Alyaarubi,
Doaa Khater,
Y. Wali,
M. Elshinawy,
Ali Almadhani,
M. Yassin,
...
A. Soliman,
D. Canatan,
Maha Obiedat,
H. Al-Rimawi,
D. Mariannis,
C. Christodoulides,
S. Christou,
Ploutarchos Tzoulis,
S. Campisi,
S. Di Maio,
V. De Sanctis
|
3 |
2019 |
3
🐜
|
|
🐢
|
A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorder
9 auth.
Alicia M Diaz-Thomas,
J. Cannon,
Pallavi Iyer,
A. Al-Maawali,
M. Fazalullah,
F. Diamond,
...
O. Mueller,
Allen W. Root,
S. Alyaarubi
|
2 |
2014 |
2
🐢
|
