The Experts below are selected from a list of 239073 Experts worldwide ranked by ideXlab platform
Harry T. Chugani - One of the best experts on this subject based on the ideXlab platform.
-
Transition into adulthood: Tuberous sclerosis complex, Sturge‐Weber syndrome, and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
-
transition into adulthood tuberous sclerosis complex sturge weber syndrome and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
-
Rasmussen encephalitis associated with parry romberg syndrome
Neurology, 2003Co-Authors: Jagdish Shah, Csaba Juhász, William J. Kupsky, Eishi Asano, Sandeep Sood, D. Fain, Harry T. ChuganiAbstract:Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscle, and bone. Occasionally, there is CNS involvement with epilepsy being the most common CNS manifestation. The authors report a child with Parry-Romberg syndrome with a course strongly suggestive of Rasmussen encephalitis. The boy underwent hemispherectomy, and pathology showed the typical findings of Rasmussen encephalitis, suggesting that these two conditions may share common etiologic factors.
-
Rasmussen encephalitis associated with Parry–Romberg syndrome
Neurology, 2003Co-Authors: Jagdish Shah, Csaba Juhász, William J. Kupsky, Eishi Asano, Sandeep Sood, D. Fain, Harry T. ChuganiAbstract:Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscle, and bone. Occasionally, there is CNS involvement with epilepsy being the most common CNS manifestation. The authors report a child with Parry-Romberg syndrome with a course strongly suggestive of Rasmussen encephalitis. The boy underwent hemispherectomy, and pathology showed the typical findings of Rasmussen encephalitis, suggesting that these two conditions may share common etiologic factors.
Elizabeth A. Thiele - One of the best experts on this subject based on the ideXlab platform.
-
Transition into adulthood: Tuberous sclerosis complex, Sturge‐Weber syndrome, and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
-
transition into adulthood tuberous sclerosis complex sturge weber syndrome and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
Sara Matricardi - One of the best experts on this subject based on the ideXlab platform.
-
Transition into adulthood: Tuberous sclerosis complex, Sturge‐Weber syndrome, and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
-
transition into adulthood tuberous sclerosis complex sturge weber syndrome and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
Tiziana Granata - One of the best experts on this subject based on the ideXlab platform.
-
Transition into adulthood: Tuberous sclerosis complex, Sturge‐Weber syndrome, and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
-
transition into adulthood tuberous sclerosis complex sturge weber syndrome and Rasmussen encephalitis
Epilepsia, 2014Co-Authors: Elizabeth A. Thiele, Tiziana Granata, Sara Matricardi, Harry T. ChuganiAbstract:Summary Children with tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis all have complex but differing needs in the process of transition/transfer to adult care. All three may be associated with long-term normal intelligence or a varying degree of intellectual disability. In tuberous sclerosis complex, the emphasis of care in adulthood shifts from seizure control and developmental issues to renal and psychiatric disease and other issues. In Sturge-Weber syndrome, the emphasis shifts from seizure control and rehabilitation to management of disability and migraine. In Rasmussen encephalitis, transition may be particularly complex for those with adolescent onset. Those successfully operated on for childhood onset have a static problem and the potential to do well in life.
Jagdish Shah - One of the best experts on this subject based on the ideXlab platform.
-
Rasmussen encephalitis associated with parry romberg syndrome
Neurology, 2003Co-Authors: Jagdish Shah, Csaba Juhász, William J. Kupsky, Eishi Asano, Sandeep Sood, D. Fain, Harry T. ChuganiAbstract:Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscle, and bone. Occasionally, there is CNS involvement with epilepsy being the most common CNS manifestation. The authors report a child with Parry-Romberg syndrome with a course strongly suggestive of Rasmussen encephalitis. The boy underwent hemispherectomy, and pathology showed the typical findings of Rasmussen encephalitis, suggesting that these two conditions may share common etiologic factors.
-
Rasmussen encephalitis associated with Parry–Romberg syndrome
Neurology, 2003Co-Authors: Jagdish Shah, Csaba Juhász, William J. Kupsky, Eishi Asano, Sandeep Sood, D. Fain, Harry T. ChuganiAbstract:Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscle, and bone. Occasionally, there is CNS involvement with epilepsy being the most common CNS manifestation. The authors report a child with Parry-Romberg syndrome with a course strongly suggestive of Rasmussen encephalitis. The boy underwent hemispherectomy, and pathology showed the typical findings of Rasmussen encephalitis, suggesting that these two conditions may share common etiologic factors.