Publications by authors named "R P Haridas"

Article Synopsis
  • Severe primary insulin-like growth factor-I deficiency (SPIGFD) is a rare disorder that leads to short stature in children due to low IGF-1 levels, and it may often go undiagnosed.* -
  • A study was conducted at a pediatric care center using an electronic medical record (EMR) algorithm to find children with short stature and low IGF-1 levels, identifying 30 potential cases of SPIGFD.* -
  • Ultimately, none of these identified patients had SPIGFD, demonstrating that the EMR algorithm can help identify children who might benefit from treatment and can be applied to other rare diseases.*
View Article and Find Full Text PDF

In mid-December 1846, British and Irish newspapers reported the news of surgical etherization far more extensively than previously described. Reports about etherization had appeared at least 20 British and Irish newspapers in the days before Robert Liston's first operations under etherization on December 21, 1846. These reports were based on four separate accounts, 2 of which could be traced to New York, and 1 account had been published in a Parisian newspaper Galignani's Messenger on December 9, 1846.

View Article and Find Full Text PDF

Background: Among youth, symptoms of depression, anxiety, and alcohol use are associated with considerable illness and disability. Youth face many personal and health system barriers in accessing mental health care. Mobile applications (apps) offer youth potentially accessible, scalable, and anonymous therapy and other support.

View Article and Find Full Text PDF

On 7 September 1847, in Melbourne in the Port Phillip District of the Colony of New South Wales, David John Thomas (1813-1871) presented a paper, 'On the inhalation of the vapour of Æther, with cases', at an ordinary monthly meeting of the Port Phillip Medical Association. This is the earliest known presentation of a paper on etherisation in Australia. The partial publication of the manuscript in October 1847 in the may have led to it being returned to Thomas in Melbourne.

View Article and Find Full Text PDF

Uterine inflammatory myofibroblastic tumors (IMTs) are rare mesenchymal neoplasms of uncertain malignant potential. Aside from the recently described risk stratification score, which has not been validated by other studies, and rare reports of aberrant p16 expression in malignant tumors, there are no criteria to reliably predict behavior. Herein, we evaluated the clinicopathologic features and p16 expression patterns in 30 IMTs, with genomic profiling performed in a subset (13 malignant, 3 benign).

View Article and Find Full Text PDF