Search

Author/Creator Alazami, Anas M.

2. ADAT3‐related intellectual disability: Further delineation of the phenotype. Issue 5 (3rd February 2016)

Authors:
El‐Hattab, Ayman W.; Saleh, Mohammed A.; Hashem, Amal; Al‐Owain, Mohammed; Asmari, Ali Al; Rabei, Hala; Abdelraouf, Hanem; Hashem, Mais; Alazami, Anas M.; Patel, Nisha; Shaheen, Ranad; Faqeih, Eissa A.; Alkuraya, Fowzan S.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 5(2016)
Page Start:
1142
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcome. Issue 6 (2nd November 2021)

Authors:
Al-Mayouf, Sulaiman M.; Alreefi, Hajar A.; Alsinan, Tuqa A.; AlSalmi, Ghada; AlRowais, Abdulaziz; Al-Herz, Waleed; Alazami, Anas M.; Alsonbul, Abdullah; Al-Mousa, Hamoud
Journal:
Modern rheumatology
Issue:
Volume 31:Issue 6(2021)
Page Start:
1171
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE. (8th November 2017)

Authors:
Al‐Mayouf, Sulaiman M.; AlSaleem, Alhanouf; AlMutairi, Nora; AlSonbul, Abdullah; Alzaid, Tariq; Alazami, Anas M.; Al‐Mousa, Hamoud
Journal:
International journal of rheumatic diseases
Issue:
Volume 21:Number 1(2018)
Page Start:
208
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Quantitative profiling of cytokines and chemokines in DOCK8‐deficient and atopic dermatitis patients. Issue 2 (15th October 2018)

Authors:
Jacob, Minnie; Bin Khalaf, Duaa; Alhissi, Safa; Arnout, Rand; Alsaud, Bander; Al‐Mousa, Hamoud; Lopata, Andreas L.; Alazami, Anas M.; Dasouki, Majed; Abdel Rahman, Anas M.
Journal:
Allergy
Issue:
Volume 74:Issue 2(2019)
Page Start:
370
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. The syndrome of deafness‐dystonia: Clinical and genetic heterogeneity. Issue 6 (15th February 2013)

Authors:
Kojovic, Maja; Pareés, Isabel; Lampreia, Tania; Pienczk‐Reclawowicz, Karolina; Xiromerisiou, Georgia; Rubio‐Agusti, Ignacio; Kramberger, Milica; Carecchio, Miryam; Alazami, Anas M.; Brancati, Francesco; Slawek, Jaroslaw; Pirtosek, Zvezdan; Valente, Enza Maria; Alkuraya, Fowzan S.; Edwards, Mark J...
Journal:
Movement disorders
Issue:
Volume 28:Issue 6(2013)
Page Start:
795
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗