Search Results - "Kupke, Kenneth G"

Effect of a Novel Oxygen Saturation Targeting Strategy on Mortality, Retinopathy of Prematurity, and Bronchopulmonary Dysplasia in Neonates Born Extremely Preterm by Srivatsa, Bharath, Malcolm, Karlous, Clark, Reese H., Kupke, Kenneth G.

“…To study the impact of an oxygen management strategy incorporating oxygen saturation (SpO2) targeting and fraction of inspired oxygen monitoring on the…”
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Oxygenation Factors Associated with Retinopathy of Prematurity in Infants of Extremely Low Birth Weight by Srivatsa, Bharath, Hagan, Joseph L., Clark, Reese H., Kupke, Kenneth G.

“…To study characteristics of oxygenation during the first 2 postnatal months and correlation with the occurrence and severity of retinopathy of prematurity…”
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Transpyloric Feeding is Associated With Improved Oxygenation Compared With Gastric Feeding Among Nonintubated Extremely Low Birth Weight Infants by Srivatsa, Bharath, Wesolowski, Agnieszka, Srivatsa, Krishna R., Bennett, Monica M., Clark, Reese H., Kupke, Kenneth G.

“…To study the impact of transpyloric (TP) feed initiation on short-term oxygenation and manual oxygen blender titration among extremely low birth weight…”
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A Modified Algorithm for Critical Congenital Heart Disease Screening Using Pulse Oximetry by Diller, Christina L, Kelleman, Michael S, Kupke, Kenneth G, Quary, Sharon C, Kochilas, Lazaros K, Oster, Matthew E

“…: media-1vid110.1542/5727212367001PEDS-VA_2017-4065 OBJECTIVES: Determine the performance of the American Academy of Pediatrics (AAP) critical congenital heart…”
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Reply by Srivatsa, Bharath, Clark, Reese H., Kupke, Kenneth G.

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Reply by Srivatsa, Bharath, Clark, Reese H, Kupke, Kenneth G

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Reply to Letter to the Editor by Srivatsa, Bharath, Clark, Reese H, Kupke, Kenneth G

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Delineation of the Dystonia-Parkinsonism Syndrome Locus in Xq13 by Graeber, Manuel B., Kupke, Kenneth G., Muller, Ulrich

“…The X chromosome-linked dystonia-parkinsonism syndrome (XDP) is a severe movement disorder, characterized by both dystonia and parkinsonism. XDP is a…”
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The phenotype of the X-linked dystonia-parkinsonism syndrome. An assessment of 42 cases in the Philippines by Lee, L V, Kupke, K G, Caballar-Gonzaga, F, Hebron-Ortiz, M, Müller, U

“…The clinical phenotype of X-linked recessive torsion dystonia was documented in 42 affected individuals from 21 families. In 7 families, there were 9 sibships…”
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Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1 by Kupke, K G, Graeber, M B, Müller, U

“…The study of rare genetic forms of dystonia and parkinsonism permits positional cloning of genes potentially involved in more common, multifactorial forms of…”
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Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis by KUPKE, K. G, LEE, L. V, MUÊLLER, U

“…We performed linkage analysis of X-linked torsion dystonia (XLTD) in 7 Filipino families, studying DNA from a total of 36 family members (9 obligate carrier…”
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The genetics of primary torsion dystonia by MUÊLLER, U, KUPKE, K. G

“…Primary torsion dystonia is an idiopathic movement disorder presumably caused by abnormal function of the basal ganglia. The disorder may be inherited either…”
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Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization by Müller, U, Schneider, N R, Marks, J F, Kupke, K G, Wilson, G N

“…An 11-year-old patient with incomplete testicular feminization and a 47,XXY karyotype is described. The patient had female external genitalia, clitoromegaly,…”
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X-linked recessive torsion dystonia in the Philippines by Kupke, K G, Lee, L V, Viterbo, G H, Arancillo, J, Donlon, T, Müller, U

“…The occurrence of an X-linked form of torsion dystonia in the Philippines was demonstrated by the genetic and biochemical analysis of affected males and their…”
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Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndrome by Kupke, K G, Soreng, A L, Müller, U

“…We report on a 10-year-old patient with the fragile X [fra(X)] syndrome and a 47,XXY karyotype. He had Martin-Bell syndrome, including typical craniofacial…”
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