1. ANKLE2‐related microcephaly: A variable microcephaly syndrome resembling Zika infection. Issue 8 (24th July 2022) Authors: Thomas, Ajay X.; Link, Nichole; Robak, Laurie A.; Demmler‐Harrison, Gail; Pao, Emily C.; Squire, Audrey E.; Michels, Savannah; Cohen, Julie S.; Comi, Anne; Prontera, Paolo; Verrotti di Pianella, Alberto; Di Cara, Giuseppe; Garavelli, Livia; Caraffi, Stefano Giuseppe; Fusco, Carlo; Zuntini, Robert... Journal: Annals of clinical and translational neurology Issue: Volume 9:Issue 8(2022) Page Start: 1276 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Antibacterial activity of novel Cu2ZnSnS4 nanoparticles against pathogenic strains. Issue 129 (15th December 2015) Authors: Kumar, R. Saravana; Maddirevula, Sateesh; Easwaran, Maheswaran; Dananjaya, S. H. S.; Kim, Moon-Deock Journal: RSC advances Issue: Volume 5:Issue 129(2015) Page Start: 106400 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. ChemInform Abstract: Antibacterial Activity of Novel Cu2ZnSnS4 Nanoparticles Against Pathogenic Strains. Issue 11 (February 2016) Authors: Kumar, R. Saravana; Maddirevula, Sateesh; Easwaran, Maheswaran; Dananjaya, S. H. S.; Kim, Moon‐Deock Journal: ChemInform Issue: Volume 47:Issue 11(2016) Page Start: no Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Confirming the involvement of PIEZO2 in the etiology of Marden–Walker syndrome. Issue 3 (27th December 2020) Authors: Seidahmed, Mohammed Zain; Maddirevula, Sateesh; Miqdad, Abeer M.; Al Faifi, Abdullah; Al Samadi, Abdulmohsen; Alkuraya, Fowzan S. Journal: American journal of medical genetics Issue: Volume 185:Issue 3(2021) Page Start: 945 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Crisponi/CISS1 syndrome: A case series. Issue 5 (24th January 2016) Authors: Alhashem, Amal M.; Majeed–Saidan, Muhammad Ali; Ammari, Amer N.; Alrakaf, Maha S.; Nojoom, Maha; Maddirevula, Sateesh; Faqeih, Eissa; Alkuraya, Fowzan S.; Garne, Ester; Kurdi, Ahmad M. Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: 1236 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Expanding the phenome and variome of skeletal dysplasia. (December 2018) Authors: Maddirevula, Sateesh; Alsahli, Saud; Alhabeeb, Lamees; Patel, Nisha; Alzahrani, Fatema; Shamseldin, Hanan; Anazi, Shams; Ewida, Nour; Alsaif, Hessa; Mohamed, Jawahir; Alazami, Anas; Ibrahim, Niema; Abdulwahab, Firdous; Hashem, Mais; Abouelhoda, Mohamed; Monies, Dorota; Al Tassan, Nada; Alshammari... Journal: Genetics in medicine Issue: Volume 20:Number 12(2018) Page Start: 1609 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Further delineation of HIDEA syndrome. Issue 12 (23rd September 2020) Authors: Maddirevula, Sateesh; Ben‐Omran, Tawfeg; AlMureikhi, Mariam; Eyaid, Wafa; Arabi, Hisham; Alkuraya, Hisham; Alfaifi, Abdullah; Alfalah, Abdullah Hamed; Alsaif, Hessa S.; Abdulwahab, Firdous; Alfadhel, Majid; Alkuraya, Fowzan S. Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 2999 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Further delineation of Temtamy syndrome of corpus callosum and ocular abnormalities. Issue 3 (31st January 2018) Authors: Alrakaf, Laila; Al‐Owain, Mohammed A.; Busehail, Maryam; Alotaibi, Maha A.; Monies, Dorota; Aldhalaan, Hesham M.; Alhashem, Amal; Al‐Hassnan, Zuhair N.; Rahbeeni, Zuhair A.; Murshedi, Fathiya Al; Ani, Nadia Al; Al‐Maawali, Almundher; Ibrahim, Niema A.; Abdulwahab, Firdous M.; Alsagob, Maysoon; Ha... Journal: American journal of medical genetics Issue: Volume 176:Issue 3(2018) Page Start: 715 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Human knockouts of PLA2G4A phenocopy NSAID-induced gastrointestinal and renal toxicity. Issue 9 (24th June 2016) Authors: Maddirevula, Sateesh; Abanemai, Mohammed; Alkuraya, Fowzan S Journal: Gut Issue: Volume 65:Issue 9(2016) Page Start: 1575 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Joint laxity in homozygotes for severe POU1F1 mutations. Issue 12 (19th August 2016) Authors: Shamseldin, Hanan E.; Maddirevula, Sateesh; Nabil, Amira; Al‐Fadhil, Saeed; Al Tala, Saeed; Alkuraya, Fowzan S. Journal: American journal of medical genetics Issue: Volume 170:Issue 12(2016) Page Start: 3356 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗