Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Eugene Garrow"'
Autor:
Rajeev Mehta, Surasak Puvabanditsin, Eugene Garrow, Melissa February, Chantal Bruno, Lissa Francois
Publikováno v:
The Cleft Palate-Craniofacial Journal. 53:249-252
The oculoauriculovertebral spectrum or Goldenhar syndrome is characterized by varying degrees of prevalently unilateral underdevelopment of the craniofacial structures (orbit, ear, and mandible) in association with vertebral, cardiac, renal, and cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e91586ea4ccc359e6abdf08d76f0f28
https://doi.org/10.1597/14-308
https://doi.org/10.1597/14-308
Publikováno v:
Pediatric emergency care. 32(11)
Ultrasound is the initial diagnostic modality of choice for evaluation of pediatric appendicitis. We report a case that highlights the importance of pain control, distraction, focusing on the appearance of the appendix and the surrounding structures,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06f9f0d28154cef23209379dc30b5935
https://pubmed.ncbi.nlm.nih.gov/26945193
https://pubmed.ncbi.nlm.nih.gov/26945193
Publikováno v:
Journal of Child Neurology. 28:124-127
We report a female infant who presented with a tail appendage bearing a gelatinous tip and an associated lipomyelocele. Magnetic resonance images revealed the presence of spina bifida and a tract in continuity from the tail to the conus medullaris. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75acc3c72d95b4d83b22a528193eedab
https://doi.org/10.1177/0883073812439436
https://doi.org/10.1177/0883073812439436
Autor:
Sharada Gowda, Eugene Garrow, Michael Nagar, Surasak Puvabanditsin, Mayoor Bhatt, Ronald Wong, Suganya Kathiravan
Publikováno v:
Fetal and Pediatric Pathology. 30:98-105
A case is described of a neonate with a four-vessel umbilical cord containing two arteries and two veins. This was due to a rare persistence of the caudal portion of the right umbilical vein. The infant had multiple congenital anomalies including a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ef96b87884ed53612db68630f278c15
https://doi.org/10.3109/15513815.2010.524687
https://doi.org/10.3109/15513815.2010.524687
Autor:
Neisha Patel, Nanthida Phattraprayoon, Alexis D'Elia, Suzanne Elizabeth Davis, Eugene Garrow, Surasak Puvabanditsin, Ahmed Zaafran
Publikováno v:
Journal of Child Neurology. 23:922-925
Monosomy 1p36 is a newly delineated multiple congenital anomalies/mental retardation syndrome characterized by mental retardation, growth delay, epilepsy, congenital heart defects, characteristic facial appearance, and precocious puberty. It is now c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52074ab2a86323c8572da850c0cbf649
https://doi.org/10.1177/0883073808314364
https://doi.org/10.1177/0883073808314364
Publikováno v:
Journal of Pediatric Surgery. 41:1822-1825
Familial cases of the various types of intestinal atresia are well described, and we now report an additional family. Based on a review of the literature, a classification system for the different types of familial atresia is presented. Current teach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee0fab0d02949b5f9ed48a19289bfae8
https://doi.org/10.1016/j.jpedsurg.2006.06.008
https://doi.org/10.1016/j.jpedsurg.2006.06.008
Autor:
Ruetima Titapiwatanakun, Jigneshkumar B. Patel, Eugene Garrow, Rahel Getachew, Surasak Puvabanditsin
Publikováno v:
Pediatric Radiology. 35:539-542
We report on an infant with severe asphyxia and persistent pulmonary hypertension as a newborn. The baby received prolonged intravenous calcium gluconate therapy for hypocalcemia. At 5 weeks of age, multiple firm, indurated areas (armor-like lesions)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::684ffd5a3791e4f136dd350e3c68ac38
https://doi.org/10.1007/s00247-004-1363-9
https://doi.org/10.1007/s00247-004-1363-9
Autor:
Passara Liangthanasarn, Angela Davydov, Eugene Garrow, Manuel Gomez, Surasak Puvabanditsin, Anjali Biswas
Publikováno v:
American Journal of Perinatology. 20:121-124
This report describes a neonate with congenital partial absence of the pericardium associated with hypoplastic left heart syndrome. The patient presented with severe heart failure caused by a hypoplastic left ventricle. The infant died at 15 hours of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4955f370b3f628a43e62e9efa3d19778
https://doi.org/10.1055/s-2003-40011
https://doi.org/10.1055/s-2003-40011
Publikováno v:
International journal of dermatology. 55(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2e001c40821e42578b97fac1d40e4f1
https://pubmed.ncbi.nlm.nih.gov/26228315
https://pubmed.ncbi.nlm.nih.gov/26228315
Publikováno v:
Journal of the American Academy of Dermatology. 44:330-335
Congenital localized absence of the skin has been observed in various subsets of inherited epidermolysis bullosa (EB). Pyloric atresia is a rare disorder that has been seen in association with EB. Ureterovesical junction obstruction is a condition un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e2127598ce9a29be01b6bf563a8530
https://doi.org/10.1067/mjd.2001.105480
https://doi.org/10.1067/mjd.2001.105480