Pober BR - Search Results

1

Ozduman K, Pober BR, Barnes P, Copel JA, Ogle EA, Duncan CC, Ment LR. Ozduman K, et al. Among authors: pober br. Pediatr Neurol. 2004 Mar;30(3):151-62. doi: 10.1016/j.pediatrneurol.2003.08.004. Pediatr Neurol. 2004. PMID: 15033196 Review.

A better understanding of those risk factors predisposing a fetus to cerebral infarction may provide a basis for future therapeutic intervention trials. Ozduman K, Pober BR, Barnes P, Copel JA, Ogle EA, Duncan CC, Ment LR. Fetal stroke....

A better understanding of those risk factors predisposing a fetus to cerebral infarction may provide a basis for future therapeutic interven …

2

Pulmonary hypoplasia and persistent pulmonary hypertension in the newborn with homozygous alpha-thalassemia: a case report and review of the literature.

Bizzarro MJ, Copel JA, Pearson HA, Pober B, Bhandari V. Bizzarro MJ, et al. J Matern Fetal Neonatal Med. 2003 Dec;14(6):411-6. doi: 10.1080/14767050412331312280. J Matern Fetal Neonatal Med. 2003. PMID: 15061322 Review.

3

Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.

Chen H, von Hehn C, Kaczmarek LK, Ment LR, Pober BR, Hisama FM. Chen H, et al. Among authors: pober br. Neurogenetics. 2007 Apr;8(2):131-5. doi: 10.1007/s10048-006-0071-z. Epub 2006 Nov 29. Neurogenetics. 2007. PMID: 17136396 Free PMC article.

4

Accuracy of fetal echocardiography.

Benacerraf BR, Pober BR, Sanders SP. Benacerraf BR, et al. Among authors: pober br. Radiology. 1987 Dec;165(3):847-9. doi: 10.1148/radiology.165.3.3685364. Radiology. 1987. PMID: 3685364

5

Association of Chiari I malformation and Williams syndrome.

Pober BR, Filiano JJ. Pober BR, et al. Pediatr Neurol. 1995 Jan;12(1):84-8. doi: 10.1016/0887-8994(94)00117-k. Pediatr Neurol. 1995. PMID: 7748369 Free article.

6

Ischemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndrome.

Soper R, Chaloupka JC, Fayad PB, Greally JM, Shaywitz BA, Awad IA, Pober BR. Soper R, et al. Among authors: pober br. J Pediatr. 1995 Jun;126(6):945-8. doi: 10.1016/s0022-3476(95)70217-2. J Pediatr. 1995. PMID: 7776102

7

Delayed diagnosis of Williams-Beuren syndrome in an adolescent of Jamaican descent: examining racial disparities in genetics education.

Gold NB, Nash KA, Perdomo J, Zheng DJ, Power-Hays A, Rainer T, Hisama F, Pober B, Feinberg E. Gold NB, et al. Clin Dysmorphol. 2021 Jan;30(1):69-70. doi: 10.1097/MCD.0000000000000357. Clin Dysmorphol. 2021. PMID: 33136657 No abstract available.

8

Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.

Mani A, Radhakrishnan J, Farhi A, Carew KS, Warnes CA, Nelson-Williams C, Day RW, Pober B, State MW, Lifton RP. Mani A, et al. Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2975-9. doi: 10.1073/pnas.0409852102. Epub 2005 Jan 31. Proc Natl Acad Sci U S A. 2005. PMID: 15684060 Free PMC article.

9

Neurologic findings in children and adults with Williams syndrome.

Chapman CA, du Plessis A, Pober BR. Chapman CA, et al. Among authors: pober br. J Child Neurol. 1996 Jan;11(1):63-5. doi: 10.1177/088307389601100116. J Child Neurol. 1996. PMID: 8745391

10

Williams syndrome--oral presentation of 45 cases.

Hertzberg J, Nakisbendi L, Needleman HL, Pober B. Hertzberg J, et al. Pediatr Dent. 1994 Jul-Aug;16(4):262-7. Pediatr Dent. 1994. PMID: 7937257 Review.

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