Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Marta Guttenberg"'
Autor:
David Watkins, Bernard S. Kaplan, Marta Guttenberg, Paige Kaplan, James R. Treat, David S. Rosenblatt, Erin A. Paul
Publikováno v:
Pediatric Nephrology. 28:1135-1139
The cblE disorder is an inherited disorder of vitamin B12 metabolism that results in elevated levels of homocysteine and decreased methionine in body fluids. Renal complications have been reported in patients with cblC disease, but not in those with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8667517c1d74e6c3ad92524b173eaf0
https://doi.org/10.1007/s00467-013-2443-6
https://doi.org/10.1007/s00467-013-2443-6
Autor:
Marta Guttenberg, Elizabeth B. Rand, Pierre Russo, Lisa M. Sullivan, Meryl S. Cohen, Rong Guo, Anitha S. John, Matthew C. Schwartz
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 143:904-909
Objective Liver fibrosis has emerged as an important long-term complication of the Fontan operation. We aimed to describe liver histology at autopsy in patients who had undergone the Fontan operation and to determine whether patient variables are ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a1a26c48fe41dd6e6d4468450648f3e
https://doi.org/10.1016/j.jtcvs.2011.08.038
https://doi.org/10.1016/j.jtcvs.2011.08.038
Publikováno v:
Fetal Diagnosis and Therapy. 24:225-229
The recent advances in neonatal and pediatric intensive care have changed the outcome of patients with congenital pulmonary lymphangiectasia of different types, including those cases with early neonatal symptoms. However, the patients who present the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b28e251bc84905c51ed9e6fa15386f1b
https://doi.org/10.1159/000151343
https://doi.org/10.1159/000151343
Autor:
Eileen M. Shore, Kareem A Zaghloul, Frederick S. Kaplan, Gregory G. Heuer, Phillip B. Storm, Marta Guttenberg
Publikováno v:
Journal of Neurosurgery: Pediatrics. 1:91-94
✓ Fibrodysplasia ossificans progressiva (FOP) is a rare, autosomal dominant disorder characterized by congenital malformation of the great toes and episodes of soft tissue swelling that lead to progressive heterotopic ossification. The genetic caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1b64c52079d60a9fb46c931116eaf38
https://doi.org/10.3171/ped-08/01/091
https://doi.org/10.3171/ped-08/01/091
Publikováno v:
Pediatric Nephrology. 22:1779-1784
Familial and genetic forms of focal segmental glomerulosclerosis (FSGS) are associated with six different mutations in genes affecting the podocyte (NPHS2, ACTN4, CD2AP, WT1, TRPC6, and PLCE1). Immunosuppressive agents are often unsuccessful in treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13bd9bb9c4736c32d0537985b9e33abd
https://doi.org/10.1007/s00467-007-0505-3
https://doi.org/10.1007/s00467-007-0505-3
Publikováno v:
Foot & Ankle International. 27:216-219
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caa3e9e5081e328b422ba3f9b6979fd9
https://doi.org/10.1177/107110070602700312
https://doi.org/10.1177/107110070602700312
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 69:567-571
To report one patient with an ectopic salivary tissue tag on the tonsil, and review the embryology, management, and implications of this benign disorder. Case report with literature review. Ectopic salivary tissue presented on the tonsil of a child a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc09afc59e92d7a077c17af913984f3a
https://doi.org/10.1016/j.ijporl.2004.11.019
https://doi.org/10.1016/j.ijporl.2004.11.019
Publikováno v:
Pediatric Nephrology. 17:800-803
Cobalamin C (cbl C) deficiency, an inherited disorder of vitamin B12 metabolism, causes elevated levels of methylmalonic acid and homocysteine and decreased methionine in all body fluids. Renal complications of cbl C disease are thrombotic microangio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c1f22cad6df08b1798c7a6a6cb0c0fb
https://doi.org/10.1007/s00467-002-0895-1
https://doi.org/10.1007/s00467-002-0895-1
Autor:
Marta Guttenberg, Faizan Alawi, Naoto Yokogawa, Scott M. Lieberman, Sharon Bout-Tabaku, Frederick B. Vivino, David D. Sherry
Publikováno v:
The Journal of rheumatology. 41(6)
Objective.To determine an appropriate focus score cutoff for childhood Sjögren syndrome (SS).Methods.Labial salivary gland tissue from specimens from children with SS and age-matched controls was retrospectively identified and reviewed by a blinded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07d7dd2c9d8aedc6faa18758d3fa8030
https://pubmed.ncbi.nlm.nih.gov/24786923
https://pubmed.ncbi.nlm.nih.gov/24786923
Publikováno v:
Pediatric Nephrology. 14:862-871
An unusual sequence of the clinical manifestations of microvascular disease is described in a 15 year-old girl. She initially presented with acute renal failure caused by a crescentic glomerulonephritis associated with positive tests for MPO-ANCA. Ei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4509aefa19ee3f3b03e9362157457f5
https://doi.org/10.1007/pl00013445
https://doi.org/10.1007/pl00013445