A Clinical Entity Often Missed—Solitary Rectal Ulcer Syndrome in Children

por Thirumal, P., Sumathi, B., Nirmala, D.
Publicado 2020

Unmasking Resident Physician Burnout During the COVID-19 Era

por Zhang, Sherry, Ramalingam, Nirmala D, Chandran, Chitra
Publicado 2023

Genetics and genomic medicine in Sri Lanka

por Sirisena, Nirmala D., Dissanayake, Vajira H. W.
Publicado 2019

Strategies for Genomic Medicine Education in Low- and Middle-Income Countries

por Sirisena, Nirmala D., Dissanayake, Vajira H. W.
Publicado 2019

Experimental Priapism is Associated with Increased Oxidative Stress and Activation of Protein Degradation Pathways in Corporal Tissue

por Kanika, Nirmala D., Melman, Arnold, Davies, Kelvin P.
Publicado 2010

The effects of meditation on length of telomeres in healthy individuals: a systematic review

por Dasanayaka, Nirodhi N., Sirisena, Nirmala D., Samaranayake, Nilakshi
Publicado 2021

Electrophoretic mobility shift assays implicate XRCC2:rs3218550C>T as a potential low-penetrant susceptibility allele for sporadic breast cancer

por Sirisena, Nirmala D., Samaranayake, Nilakshi, Dissanayake, Vajira H. W.
Publicado 2019

Implementation of genomic medicine in Sri Lanka: Initial experience and challenges

por Sirisena, Nirmala D., Neththikumara, Nilaksha, Wetthasinghe, Kalum, Dissanayake, Vajira H.W.
Publicado 2016

Improving Internal Medicine Residents’ Comfort Managing Psychiatric Conditions Through an Interactive, Case-Based Workshop

por Patel, Rushi, Ramalingam, Nirmala D., Pal, Anish, Tran, H. Nicole, Hirschtritt, Matthew E.
Publicado 2023

Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer

por Gunawardena, Kawmadi, Sirisena, Nirmala D., Anandagoda, Gayani, Neththikumara, Nilaksha, Dissanayake, Vajira H.W.
Publicado 2023

Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations

por Sirisena, Nirmala D., Wijetunge, U. Kalpani S., de Silva, Ramya, Dissanayake, Vajira H. W.
Publicado 2013

The Frequency and Spectrum of Chromosomal Translocations in a Cohort of Sri Lankans

por Paththinige, Chamara S., Sirisena, Nirmala D., Kariyawasam, U. G. I. U., Dissanayake, Vajira H. W.
Publicado 2019

SUN-025 Obesity Severity and Polycystic Ovary Syndrome in an Ethnically Diverse Cohort of Adolescent Girls

por Khil, Jaclyn, Chandra, Malini, Ramalingam, Nirmala D, Greenspan, Louise C, Lo, Joan Chia-Mei
Publicado 2020

A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development

por Wettasinghe, Kalum T., Sirisena, Nirmala D., Andraweera, Prabha H., Jayasekara, Rohan W., Dissanayake, Vajira H. W.
Publicado 2012

AB302. SPR-29 Sphingosine-1-phosphate in vitro and in vivo modulates corpus cavernosum smooth muscle tone

por Zhang, Xinhua, Yin, Jing, Kanika, Nirmala D., Tong, Yuehong, Villegas, Guillermo, Melman, Arnold, DiSanto, Michael E.
Publicado 2016

Prevalence of prediabetes and diabetes vary by ethnicity among U.S. Asian adults at healthy weight, overweight, and obesity ranges: an electronic health record study

por Vicks, William S., Lo, Joan C., Guo, Lynn, Rana, Jamal S., Zhang, Sherry, Ramalingam, Nirmala D., Gordon, Nancy P.
Publicado 2022

Effectiveness of a pharmacist-led quality improvement program to reduce medication errors during hospital discharge

por George, Doris, Supramaniam, Nirmala D., Hamid, Siti Q. Abd, Hassali, Mohamad A., Lim, Wei-Yin, Hss, Amar-Singh
Publicado 2019

Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature

por Joseph, Anne D. D., Sirisena, Nirmala D., Kumanan, Thirunavukarasu, Sujanitha, Vathualan, Strelow, Veronika, Yamamoto, Raina, Wieczorek, Stefan, Dissanayake, Vajira H. W.
Publicado 2019

Mass Spectrometric Imaging of the Brain Demonstrates the Regional Displacement of 6-Monoacetylmorphine by Naloxone

por Teklezgi, Belin G., Pamreddy, Annapurna, Ntshangase, Sphamandla, Mdanda, Sipho, Singh, Sanil D., Gopal, Nirmala D., Naicker, Tricia, Kruger, Hendrik G., Govender, Thavendran, Baijnath, Sooraj
Publicado 2020

A recurrent homozygous missense DPM3 variant leads to muscle and brain disease

por Nagy, Sara, Lau, Tracy, Alavi, Shahryar, Karimiani, Ehsan Ghayoor, Vallian, Jalal, Ng, Bobby G., Noroozi Asl, Samaneh, Akhondian, Javad, Bahreini, Amir, Yaghini, Omid, Uapinyoying, Prech, Bonnemann, Carsten, Freeze, Hudson H., Dissanayake, Vajira H. W., Sirisena, Nirmala D., Schmidts, Miriam, Houlden, Henry, Moreno‐De‐Luca, Andres, Maroofian, Reza
Publicado 2022