Female genital tuberculosis and infertility: serial cases report in Bandung, Indonesia and literature review

Por Djuwantono, Tono, Permadi, Wiryawan, Septiani, Leri, Faried, Ahmad, Halim, Danny, Parwati, Ida
Publicado no BMC Res Notes (2017)

Risk of neurodevelopmental disorders in children born from different ART treatments: a systematic review and meta-analysis

Por Djuwantono, Tono, Aviani, Jenifer Kiem, Permadi, Wiryawan, Achmad, Tri Hanggono, Halim, Danny
Publicado no J Neurodev Disord (2020)

A comparison of cryopreservation methods: Slow-cooling vs. rapid-cooling based on cell viability, oxidative stress, apoptosis, and CD34(+ )enumeration of human umbilical cord blood...

Por Djuwantono, Tono, Wirakusumah, Firman F, Achmad, Tri H, Sandra, Ferry, Halim, Danny, Faried, Ahmad
Publicado em 2011

Potency of Mesenchymal Stem Cell and Its Secretome in Treating COVID-19

Por Chouw, Angliana, Milanda, Tiana, Sartika, Cynthia Retna, Kirana, Marsya Nilam, Halim, Danny, Faried, Ahmad
Publicado no Regen Eng Transl Med (2021)

The neurological significance of COVID-19: Lesson learn from the pandemic

Por Faried, Ahmad, Dian, Sofiati, Halim, Danny, Hermanto, Yulius, Pratama, Dilli Marayuzan Akbar, Arifin, Muhammad Zafrullah
Publicado no Interdiscip Neurosurg (2020)

Correlation between the skull base fracture and the incidence of intracranial hemorrhage in patients with traumatic brain injury

Por Faried, Ahmad, Halim, Danny, Widjaya, Ingrid Ayke, Badri, Rendy Febrian, Sulaiman, Syailendra Fii, Arifin, Muhammad Z.
Publicado no Chin J Traumatol (2019)

The Direct Inhibitory Effect of Dutasteride or Finasteride on Androgen Receptor Activity is Cell Line Specific

Por Chhipa, Rishi Raj, Halim, Danny, Cheng, Jinrong, Zhang, Huan Yi, Mohler, James L., Ip, Clement, Wu, Yue
Publicado em 2013

Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins

Por Zuris, John A., Halim, Danny A., Conlan, Andrea R., Abresch, Edward C., Nechushtai, Rachel, Paddock, Mark L., Jennings, Patricia A.
Publicado em 2010

Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

Por Alves, Maria M, Halim, Danny, Maroofian, Reza, de Graaf, Bianca M, Rooman, Raoul, van der Werf, Christine S, Van de Vijver, Els, Mehrjardi, Mohammad YV, Aflatoonian, Majid, Chioza, Barry A, Baple, Emma L, Dehghani, Mohammadreza, Crosby, Andrew H, Hofstra, Robert MW
Publicado no Eur J Hum Genet (2016)

Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Por Halim, Danny, Brosens, Erwin, Muller, Françoise, Wangler, Michael F., Beaudet, Arthur L., Lupski, James R., Akdemir, Zeynep H. Coban, Doukas, Michael, Stoop, Hans J., de Graaf, Bianca M., Brouwer, Rutger W.W., van Ijcken, Wilfred F.J., Oury, Jean-François, Rosenblatt, Jonathan, Burns, Alan J., Tibboel, Dick, Hofstra, Robert M.W., Alves, Maria M.
Publicado no Am J Hum Genet (2017)

Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice

Por Halim, Danny, Wilson, Michael P., Oliver, Daniel, Brosens, Erwin, Verheij, Joke B. G. M., Han, Yu, Nanda, Vivek, Lyu, Qing, Doukas, Michael, Stoop, Hans, Brouwer, Rutger W. W., van IJcken, Wilfred F. J., Slivano, Orazio J., Burns, Alan J., Christie, Christine K., de Mesy Bentley, Karen L., Brooks, Alice S., Tibboel, Dick, Xu, Suowen, Jin, Zheng Gen, Djuwantono, Tono, Yan, Wei, Alves, Maria M., Hofstra, Robert M. W., Miano, Joseph M.
Publicado no Proc Natl Acad Sci U S A (2017)