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Tomorrow's Leaders
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Sonia Partap, MD, monitors Marcos Mendoza's progress as he recovers from neurosurgery to treat a brain tumor. The excercises allow her to measure improvements in his hand-eye coordination. |
For as long as she can remember, Sonia Partap has wanted to be a doctor. "My parents are physicians from India," says the St. Louis native. "My father is a psychiatrist, my mother is a pathologist, and my sister was in medical school when I was in high school, so growing up I was surrounded by medicine."
While completing a combined BA/MD degree program at the University of Missouri-Kansas City, Partap began gravitating toward pediatrics. "Kids are much more resilient than adults," she says. "I was inspired by their spirit."
After graduating from medical school in 2000, Partap entered a two-year residency program in pediatrics at Brown University, followed by a three-year residency in adult and child neurology at the University of Washington in Seattle. In 2005, she was selected as the first Beverly and Bernard Wolfe Fellow in Neuro-oncology at Stanford, a three-year fellowship supervised by Paul Fisher, MD, the Beirne Family Director of Neuro-Oncology at Packard Hospital.
"Sonia has superb clinical acumen and great compassion," says Fisher. "The Wolfe fellowship has allowed her to take on novel interdisciplinary training in oncology, radiology, radiation oncology, and pathology, which will put her far ahead of other clinicians starting their careers in pediatric neuro-oncology. With such unique clinical experience and some additional training to come in epidemiology research, we are preparing Sonia to become a leader in the field in years to come."
"Brain tumors are one of the most common childhood cancers and, sadly, are the leading cause of cancer deaths in children," says Partap. "The development of effective new therapies will require improved diagnostic methods, increased understanding of tumor biology and risk factors, and novel clinical trial strategies. The Wolfe fellowship has provided me an unparalleled opportunity to develop the skills that I will need as I begin a clinical research career in pediatric neuro-oncology."
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Carolyn Chi, MD, examines Gabriel Sanchez in the endocrinology clinic. The 10-year-old from Modesto received a pacemaker inplant to treat his heart condition and visits Packard regularly where doctors monitor his growth and development. |
Carolyn Chi's passion for public health was kindled during her undergraduate years at Rice University. "I was majoring in sociology and biology and began doing research on the health care needs of AIDS hospice patients," she recalls. "It was a sociology professor who encouraged me to go into medicine."
She eventually enrolled at Stanford Medical School and began focusing on children's health. "I prefer working with kids," she says. "They're very true patients. When they feel better, you know it: They're up playing, and they want to go home."
In 2004, after four years of medical school and three years of residency training at Packard Hospital, Chi accepted a three-year fellowship in pediatric endocrinology, a subspecialty that focuses on glandular and metabolic disorders in children.
"The first year of my fellowship was funded by the Department of Pediatrics," she says. "I was fortunate to obtain an Arline and Pete Harman Fellowship for the final two years. Without it, I'd still be applying for grants and trying to get funding."
One of Chi's main areas of research is childhood obesity. "During my fellowship, I've been conducting a study on insulin resistance in obese adolescents with Darrell Wilson, MD, chief of pediatric endocrinology at Packard. There are a number of obesity-related health problems associated with insulin resistance, including type 2 diabetes, high blood pressure, and irregular menstrual periods."
Chi also has been collaborating with E. Kirk Neely, MD, clinical associate professor of pediatrics, on a study evaluating the treatment of central precocious puberty--a pituitary gland disorder that triggers early puberty in children younger than 8. "The ultimate consequence for these kids is short stature," she explains. "Without treatment, a child may end up significantly shorter than their projected genetic height."
The cause of central precocious puberty remains a mystery--one of many challenges that led Chi to pursue a fellowship in pediatric endocrinology. "Without fellowship training programs, there is no pipeline to produce specialists," she says. "So I'm extremely grateful to the Harmans and other donors. Ultimately, they're training doctors who will have the clinical skills to care for children with special needs and advance the field of medicine."
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One-year-old Gurshan Kaur-Gill, from Bakersfield, gets a check up from biochemical geneticist Gregory Enns, MD. The toddler suffers from an inherited metabolic disorder that can affect mitochondrial function in his cells. |
When it comes to pediatric subspecialists, Gregory Enns, MD, is virtually in a class by himself. Enns is a biochemical geneticist--the only one at Packard and one of only a handful in California. He studies mitochondrial diseases: genetic disorders that interfere with energy-producing parts of the cell known as mitochondria. Each year, hundreds of children in the United States are born with mitochondrial diseases, often with devastating symptoms, such as mental retardation, seizures, deafness, heart damage, and liver failure.
"Mitochondria are basically cellular engines," says Enns, an associate professor of pediatrics, who joined the Stanford faculty in 1998. "They are critical for energy metabolism in all parts of our body, and they have been implicated in almost every disease process we know of--diabetes, cancer, neurodegenerative disorders, even aging. They also can be extremely hard to diagnose and treat."
In 2006, Enns was named an Arline and Pete Harman Faculty Scholar. This special award provides Enns with three years of financial support to study new ways to identify and treat these illnesses.
"As a faculty scholar, I can devote more time to science and research," he says. "The thrust of my work has to do with the fact that mitochondria not only generate energy for the cell, they also produce toxins, just like a car engine produces exhaust," he explains. "If mitochondria don't work right, they produce a lot of biochemical exhaust."
The presence of toxic molecules in the bloodstream may be an indication of mitochondrial disease, he says. His goal is to develop a state-of-the-art blood test to detect these toxic biomarkers, giving pediatricians a reliable method of detecting and monitoring the severity of a child's mitochondrial diseases. Such a test also could be used to determine the efficacy of treatment.
"Right now it is very difficult to determine how well a given treatment works," Enns says. "We'd like to have something that we can monitor and quantify, and with our biomarkers, I think we're onto something. I would say that support like the Harman Faculty Scholar Fund is absolutely critical, because it allows me to conduct translational research that can really have an effect on children's lives."
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