ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease von Suleiman, Jehan, Hamwi, Nadia, El-Hattab, Ayman W.

Volltext

Stenotrophomonas maltophilia Meningitis in a Term Healthy Neonate: A Case Report and Literature Review von Al-Dulaimi, Zahraa, Abdelghafar, Mohamed, Rabei, Hala, Hamwi, Nadia, Ibrahim, Judy, Al Tatari, Hossam

Volltext

Two cases of carbonic anhydrase VA deficiency—An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcome von Marwaha, Ashish, Ibrahim, Judy, Rice, Taylor, Hamwi, Nadia, Rupar, Charles Anthony, Cresswell, David, Prasad, Chitra, Schulze, Andreas

Volltext

Two cases of carbonic anhydrase VA deficiency-An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcome von Marwaha, Ashish, Ibrahim, Judy, Rice, Taylor, Hamwi, Nadia, Rupar, Charles Anthony, Cresswell, David, Prasad, Chitra, Schulze, Andreas

Volltext

Stenotrophomonas maltophilia Meningitis in a Term Healthy Neonate: A Case Report and Literature Review von Ibrahim, Judy, Hamwi, Nadia, Rabei, Hala, Abdelghafar, Mohamed, Al-Dulaimi, Zahraa, Al Tatari, Hossam

Volltext

Influence of parental knowledge and attitudes on the oral and dental health status of autistic children: A systematic review von Salmeh, Abdulrahman, Al-Saadi, Meena, AlZaidi, Nadia, Al Hamwi, Noura, Jumaah, Sarah Safaa, Karimzadeh, Shamma, Dhafer, Taiba, Al-Rubaiay, Ward, Al-Rawi, Natheer

Volltext