Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bhavna Bali"'
Autor:
Christianne J. Lane, Mitchell E. Geffner, Sandra Hall, Ashley H. Park, Bhavna Bali, Mimi S. Kim, Anna Ryabets-Lienhard
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 99:E1597-E1601
Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency can cause life-threatening adrenal crises as well as severe hypoglycemia, especially in very young children. Studies of CAH patients 4 years old or older have found abnor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df56ba42993817fdcbd46c0c1c51b1e1
https://doi.org/10.1210/jc.2014-1274
https://doi.org/10.1210/jc.2014-1274
Autor:
David A. Greenberg, Zeynep Baskurt, Patricia McGoldrick, Theodore Chiang, Huntley Hardison, Bhavna Bali, Tara Clarke, Ruslan Dorfman, Steven M Wolf, Weili Li, Steven L. Kugler, Deb K. Pal, Edward J. Novotny, Elaine C. Wirrell, James J. Russo, Minchen Chien, Lisa J. Strug, Jingyue Ju, David E. Mandelbaum
Publikováno v:
European Journal of Human Genetics. 17:1171-1181
Rolandic epilepsy (RE) is the most common human epilepsy, affecting children between 3 and 12 years of age, boys more often than girls (3:2). Focal sharp waves in the centrotemporal area define the electroencephalographic (EEG) trait for the syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::647f656328ac93afdb35f415151a62d9
https://doi.org/10.1038/ejhg.2008.267
https://doi.org/10.1038/ejhg.2008.267
Autor:
Bhavna Bali, Lisa J. Strug, P. L. Murphy, Deb K. Pal, Steven L. Kugler, David A. Greenberg, Bernadine R. Gagnon, Tara Clarke, Philip Lieberman
Publikováno v:
Epilepsia. 49:1086-1090
We report a three generation pedigree with 11 of 22 affected with a variant form of rolandic epilepsy, speech impairment, oromotor apraxia, and cognitive deficit. The core features comprised nocturnal rolandic seizures, interictal centrotemporal spik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4641a43074c5177bae2aaff1cef80aa2
https://doi.org/10.1111/j.1528-1167.2007.01517.x
https://doi.org/10.1111/j.1528-1167.2007.01517.x
Publikováno v:
Dermato-Endocrinology. 3:230-232
To our knowledge there have been no reports of scleroderma-like skin changes, not affecting the hand in prepubertal patients with Type I Diabetes Mellitus (T1DM). We report a prepubertal caucasian male with T1DM, and early morphea-type skin changes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfedcb1809c4a98a2ef97287554ebd9
https://doi.org/10.4161/derm.3.4.14614
https://doi.org/10.4161/derm.3.4.14614
Autor:
Bhavna Bali, David A. Greenberg, Tara Clarke, Lisa J. Strug, P. L. Murphy, Lewis L. Kull, Deb K. Pal, Cigdem I. Akman
Publikováno v:
Epilepsia. 48(12)
SUMMARY Purpose: Centrotemporal sharp (CTS) waves, the electroencephalogram (EEG) hallmark of rolandic epilepsy, are found in approximately 4% of the childhood population. The inheritance of CTS is presumed autosomal dominant but this is controversia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::538deace7b7db267bd5758ec028f0fd1
https://pubmed.ncbi.nlm.nih.gov/17662063
https://pubmed.ncbi.nlm.nih.gov/17662063
Summary Rolandic epilepsy (RE) is designated an idiopathic epilepsy syndrome, and hence no lesional abnormalities are expected on MRI exam. Recent reports suggest that MRI abnormalities are not only common, but may be specific for temporal lobe epile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbd2e1c6224cf595f997db6e24396e65
https://europepmc.org/articles/PMC2001310/
https://europepmc.org/articles/PMC2001310/
Publikováno v:
Annals of Neurology. 57:464-465
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fa3c836b8e028a7f26535d38e675000
https://doi.org/10.1002/ana.20399
https://doi.org/10.1002/ana.20399
Publikováno v:
Annals of Neurology; Mar2005, Vol. 57 Issue 3, p464-465, 2p