Current Screening Strategies for the Diagnosis of Adrenal Insufficiency in Children

por Bowden, Sasigarn A
Publicado 2023

Pediatric Adrenal Insufficiency: Diagnosis, Management, and New Therapies

por Bowden, Sasigarn A., Henry, Rohan
Publicado 2018

Chronic Bilateral Slipped Capital Femoral Epiphysis as an Unusual Presentation of Congenital Panhypopituitarism due to Pituitary Hypoplasia in a 17-Year-Old Female

por Bowden, Sasigarn A., Klingele, Kevin E.
Publicado 2009

Adrenal Function Testing Following Hormone Therapy for Infantile Spasms: Case Series and Review of Literature

por Mytinger, John R., Bowden, Sasigarn A.
Publicado 2015

Profile of asfotase alfa in the treatment of hypophosphatasia: design, development, and place in therapy

por Bowden, Sasigarn A, Foster, Brian L
Publicado 2018

Optimizing Bone Health in Duchenne Muscular Dystrophy

por Buckner, Jason L., Bowden, Sasigarn A., Mahan, John D.
Publicado 2015

Repeating ACTH Stimulation Test Is Necessary to Diagnose ACTH Deficiency in Neonatal Hypopituitarism With Initial False Negative Result

por Coshway, Loyal K., Indyk, Justin A., Bowden, Sasigarn A.
Publicado 2014

Management of Adrenal Insufficiency Risk After Long-term Systemic Glucocorticoid Therapy in Duchenne Muscular Dystrophy: Clinical Practice Recommendations

por Bowden, Sasigarn A., Connolly, Anne M., Kinnett, Kathi, Zeitler, Philip S.
Publicado 2019

Successful Medical Therapy for Hypophosphatemic Rickets due to Mitochondrial Complex I Deficiency Induced de Toni-Debré-Fanconi Syndrome

por Bowden, Sasigarn A., Patel, Hiren P., Beebe, Allan, McBride, Kim L.
Publicado 2013

Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy

por Bowden, Sasigarn A., Cozzi, Corin, Hickey, Scott E., Thrush, Devon Lamb, Astbury, Caroline, Nuthakki, Sushma
Publicado 2013

Mineralization Defects in the Primary Dentition Associated With X‐Linked Hypophosphatemic Rickets

por Clayton, Delaney, Chavez, Michael B, Tan, Michelle H, Kolli, Tamara N, Giovani, Priscila A, Hammersmith, Kimberly J, Bowden, Sasigarn A, Foster, Brian L
Publicado 2021

Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases

por Zhou, Danlei, Rudnicki, Michael, Chua, Gilbert T., Lawrance, Simon K., Zhou, Bi, Drew, Joanne L., Barbar-Smiley, Fatima, Armstrong, Taylor K., Hilt, Miranda E., Birmingham, Daniel J., Passler, Werner, Auletta, Jeffrey J., Bowden, Sasigarn A., Hoffman, Robert P., Wu, Yee Ling, Jarjour, Wael N., Mok, Chi Chiu, Ardoin, Stacy P., Lau, Yu Lung, Yu, Chack Yung
Publicado 2021

POLRMT mutations impair mitochondrial transcription causing neurological disease

por Oláhová, Monika, Peter, Bradley, Szilagyi, Zsolt, Diaz-Maldonado, Hector, Singh, Meenakshi, Sommerville, Ewen W., Blakely, Emma L., Collier, Jack J., Hoberg, Emily, Stránecký, Viktor, Hartmannová, Hana, Bleyer, Anthony J., McBride, Kim L., Bowden, Sasigarn A., Korandová, Zuzana, Pecinová, Alena, Ropers, Hans-Hilger, Kahrizi, Kimia, Najmabadi, Hossein, Tarnopolsky, Mark A., Brady, Lauren I., Weaver, K. Nicole, Prada, Carlos E., Õunap, Katrin, Wojcik, Monica H., Pajusalu, Sander, Syeda, Safoora B., Pais, Lynn, Estrella, Elicia A., Bruels, Christine C., Kunkel, Louis M., Kang, Peter B., Bonnen, Penelope E., Mráček, Tomáš, Kmoch, Stanislav, Gorman, Gráinne S., Falkenberg, Maria, Gustafsson, Claes M., Taylor, Robert W.
Publicado 2021