Pablo Altschwager
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Explore the profile of Pablo Altschwager including associated specialties, affiliations and a list of published articles.
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9
Citations
41
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0
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Recent Articles
1.
Altamirano F, Hoyek S, Savant S, De Bruyn H, Altschwager P, Oke I, et al.
J AAPOS
. 2024 Sep;
28(5):104005.
PMID: 39313090
Purpose: To describe the clinical characteristics and outcomes of children with posterior segment coloboma (PSC). Methods: The medical records of children (age <18 years) with PSC examined at Boston Children's...
2.
Teng R, Nguyen M, Hunter D, Altschwager P
J AAPOS
. 2024 Sep;
28(5):103996.
PMID: 39299511
Fluorescein angiography is a fluorescent dye-based imaging procedure, most commonly indicated in the pediatric setting to evaluate peripheral retinal vascular lesions. Fluorescein dye is organic, water soluble, and largely excreted...
3.
Ayash J, Woods R, Akula J, Rajabi F, Alwattar B, Altschwager P, et al.
Am J Ophthalmol
. 2024 Mar;
263:168-178.
PMID: 38461945
Purpose: To evaluate ocular and retinal features of CRB1-associated early onset severe retinal dystrophy/Leber congenital amaurosis (EOSRD/LCA) for age-related changes. Design: Retrospective cohort study. Methods: Sixteen pediatric patients with biallelic...
4.
Fonseca M, Nouck-A-Nwal A, Ambrosio L, Altschwager P, Hansen R, Fulton A, et al.
Doc Ophthalmol
. 2022 May;
145(1):1-10.
PMID: 35536490
Purpose: To determine the association of the multifocal electroretinographic (mfERG) response amplitude with the volumes of the inner, postreceptor, and photoreceptor retinal layers in the region stimulated by each mfERG...
5.
Altschwager P, Ambrosio L, Swanson E, Moskowitz A, Fulton A
Semin Pediatr Neurol
. 2017 Sep;
24(2):104-109.
PMID: 28941524
In this article, we review the following 3 common juvenile macular degenerations: Stargardt disease, X-linked retinoschisis, and Best vitelliform macular dystrophy. These are inherited disorders that typically present during childhood,...
6.
Altschwager P, Moskowitz A, Fulton A, Hansen R
Invest Ophthalmol Vis Sci
. 2017 May;
58(5):2603-2608.
PMID: 28494494
Purpose: The purpose of this study is to assess cone-mediated central retinal function in children with a history of preterm birth, including subjects with and without retinopathy of prematurity (ROP)....
7.
Gradstein L, Hansen R, Cox G, Altschwager P, Fulton A
Doc Ophthalmol
. 2017 Feb;
134(2):135-140.
PMID: 28144890
Purpose: We report for the first time electroretinographic (ERG) evidence of progressive retinal abnormalities in a girl who presented in infancy with ocular features of albinism and gradually developed choroidal...
8.
Lamont R, Tan W, Innes A, Parboosingh J, Schneidman-Duhovny D, Rajkovic A, et al.
Eur J Hum Genet
. 2016 Mar;
24(10):1436-44.
PMID: 27004616
Sequence variants in CRB2 cause a syndrome with greatly elevated maternal serum alpha-fetoprotein and amniotic fluid alpha-fetoprotein levels, cerebral ventriculomegaly and renal findings similar to Finnish congenital nephrosis. All reported...
9.
Norero E, Altschwager P, Romero C, Mellado P, Hernandez G, Castillo L, et al.
Rev Med Chil
. 2004 Sep;
132(1):11-8.
PMID: 15379047
Background: The need of mechanical ventilation among patients with acute neurological diseases is considered a poor prognostic sign. Aim: To determine the mortality and functional recovery of neurological patients requiring...