Mary B. Davis - Publications, H-index & Citations

Mary B. Davis

university of iowa college of nursing

48H指数

160论文数

7.0K被引数

收录论文 59

发表时间

Caring for the child with intestinal failure on home parenteral nutrition: A scoping review 对接受家庭肠外营养支持的肠衰竭患儿的护理：一项范围综述

Journal of Parenteral and Enteral Nutrition

IF4.1

2025-11-07

OAAI

Mary Beth Hovda Davis PhD; Valerie Boebel Toly PhD; Erin Weber MSN; Riad Rahhal MD; Ann Marie McCarthy PhD

Limiting Central Venous Catheter Access for Blood Sampling and its Impact on Central Line-associated blood stream infection: A Scoping Review 限制中心静脉导管通路用于血液采样及其对中心静脉导管相关血流感染的影响：一项范围综述

American Journal of Infection Control

IF2.4

2025-11-04

PREAI

Mary Beth Hovda Davis; Takaaki Kobayashi; Kathryn Trautman; Karen Brust

'Dementia has got two faces': grief as an experience of holding on and letting go for people living with primary progressive aphasia and posterior cortical atrophy “痴呆症具有两面性”：对于患有进行性失语症和后部皮质萎缩的人群而言，悲伤是一种坚持与放手并存的经历。

AGING & MENTAL HEALTH

IF2.4

2025-05-18

OAAI

Waddington, C; Clements, H; Crutch, S; Davis, M; Glenister, J; Harding, E; Thompson, EH; Walton, J; Stott, J

Descriptive epidemiology of central line-associated bloodstream infections at an academic medical center in Iowa, 2019-2022

AMERICAN JOURNAL OF INFECTION CONTROL

IF2.4

2024-04-01

PREAI

Harrington, Elaine M.; Trautman, Kathryn; Davis, Mary B.; Varzavand, Kristin; Meacham, Holly; Dains, Angelique; Marra, Alexandre R.; Mcdanel, Jennifer; Kenne, Lynnette; Hanna, Beth; Murphy, Jaime P.; Diekema, Daniel J.; Wellington, Melanie; Brust, Karen B.; Kobayashi, Takaaki; Abosi, Oluchi J.

Characteristics, Comorbidities, and Data Gaps for Coronavirus Disease Deaths, Tennessee, USA

EMERGING INFECTIOUS DISEASES

IF6.6

2021-10-01

OAAI

Parker, John James; Octaria, Rany; Smith, Miranda D.; Chao, Samantha J.; Davis, Mary Beth; Goodson, Celia; Warkentin, Jon; Werner, Denise; Fill, Mary-Margaret A.

Impact of central venous catheter repair in pediatric intestinal failure

JOURNAL OF PARENTERAL AND ENTERAL NUTRITION

IF4.1

2021-04-20

PREAI

Santhana, Velarchana; Davis, Mary Beth; Rahhal, Riad

Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17 脊髓小脑共济失调的遗传学和临床表现的复杂性17

FRONTIERS IN CELLULAR NEUROSCIENCE

IF4

2018-11-23

OAAI

Nethisinghe, Suran; Lim, Wei N.; Ging, Heather; Zeitlberger, Anna; Abeti, Rosella; Pemble, Sally; Sweeney, Mary G.; Labrum, Robyn; Cervera, Charisse; Houlden, Henry; Rosser, Elisabeth; Limousin, Patricia; Kennedy, Angus; Lunn, Michael P.; Bhatia, Kailash P.; Wood, Nicholas W.; Hardy, John; Polke, James M.; Veneziano, Liana; Brusco, Alfredo; Davis, Mary B.; Giunti, Paola

PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption

FRONTIERS IN CELLULAR NEUROSCIENCE

IF4

2018-07-31

OAAI

Nethisinghe, Suran; Pigazzini, Maria Lucia; Pemble, Sally; Sweeney, Mary G.; Labrum, Robyn; Manso, Katarina; Moore, David; Warner, Jon; Davis, Mary B.; Giunti, Paola

Outcomes of Patients Receiving Temporary Circulatory Support Before Durable Ventricular Assist Device

ANNALS OF THORACIC SURGERY

IF3.9

2017-01-01

OAAI

Shah, Palak; Pagani, Francis D.; Desai, Shashank S.; Rongione, Anthony J.; Maltais, Simon; Haglund, Nicholas A.; Dunlay, Shannon M.; Aaronson, Keith D.; Stulak, John M.; Davis, Mary Beth; Salerno, Christopher T.; Cowger, Jennifer A.

A multi-institutional outcome analysis of patients undergoing left ventricular assist device implantation stratified by sex and race

JOURNAL OF HEART AND LUNG TRANSPLANTATION

IF6

2017-01-01

PREAI

van Meeteren, Justin; Maltais, Simon; Dunlay, Shannon M.; Haglund, Nicholas A.; Davis, Mary Beth; Cowger, Jennifer; Shah, Palak; Aaronson, Keith D.; Pagani, Francis D.; Stulak, John M.

Prevalence study of genetically defined skeletal muscle channelopathies in England

NEUROLOGY

IF8.5

2013-04-16

OAAI

Horga, Alejandro; Rayan, Dipa L. Raja; Matthews, Emma; Sud, Richa; Fialho, Doreen; Durran, Siobhan C. M.; Burge, James A.; Portaro, Simona; Davis, Mary B.; Haworth, Andrea; Hanna, Michael G.

Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia

ANNALS OF NEUROLOGY

IF7.7

2013-02-19

140

OAAI

Hersheson, Joshua; Mencacci, Niccolo E.; Davis, Mary; MacDonald, Nicola; Trabzuni, Daniah; Ryten, Mina; Pittman, Alan; Paudel, Reema; Kara, Eleanna; Fawcett, Katherine; Plagnol, Vincent; Bhatia, Kailash P.; Medlar, Alan J.; Stanescu, Horia C.; Hardy, John; Kleta, Robert; Wood, Nicholas W.; Houlden, Henry

A new explanation for recessive myotonia congenita Exon deletions and duplications in CLCN1

NEUROLOGY

IF8.5

2012-06-12

OAAI

Rayan, D. L. Raja; Haworth, A.; Sud, R.; Matthews, E.; Fialho, D.; Burge, J.; Portaro, S.; Schorge, S.; Tuin, K.; Lunt, P.; McEntagart, M.; Toscano, A.; Davis, M. B.; Hanna, M. G.

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

IF7.5

2012-05-10

292

OAAI

Murphy, Sinead M.; Laura, Matilde; Fawcett, Katherine; Pandraud, Amelie; Liu, Yo-Tsen; Davidson, Gabrielle L.; Rossor, Alexander M.; Polke, James M.; Castleman, Victoria; Manji, Hadi; Lunn, Michael P. T.; Bull, Karen; Ramdharry, Gita; Davis, Mary; Blake, Julian C.; Houlden, Henry; Reilly, Mary M.

IDENTIFYING THE CAUSE OF PHENOTYPIC VARIABILITY IN A FAMILY WITH NON-DYSTROPHIC MYOTONIA

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

IF7.5

2012-02-09

PREAI

Rayan, D. Raja; Haworth, A.; Sud, R.; McCall, S.; Tan, S. V.; Durran, S.; Davis, M.; Hanna, M. G.

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

NEUROLOGY

IF8.5

2011-11-29

OAAI

Matthews, E.; Portaro, S.; Ke, Q.; Sud, R.; Haworth, A.; Davis, M. B.; Griggs, R. C.; Hanna, M. G.

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

NEUROLOGY

IF8.5

2011-07-12

OAAI

Polke, J. M.; Laura, M.; Pareyson, D.; Taroni, F.; Milani, M.; Bergamin, G.; Gibbons, V. S.; Houlden, H.; Chamley, S. C.; Blake, J.; DeVile, C.; Sandford, R.; Sweeney, M. G.; Davis, M. B.; Reilly, M. M.

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology Dravet综合征作为癫痫性脑病: 长期病程和神经病理学的证据

BRAIN

IF11.7

2011-06-29

188

OAAI

Catarino, Claudia B.; Liu, Joan Y. W.; Liagkouras, Ioannis; Gibbons, Vaneesha S.; Labrum, Robyn W.; Ellis, Rachael; Woodward, Cathy; Davis, Mary B.; Smith, Shelagh J.; Cross, J. Helen; Appleton, Richard E.; Yendle, Simone C.; McMahon, Jacinta M.; Bellows, Susannah T.; Jacques, Thomas S.; Zuberi, Sameer M.; Koepp, Matthias J.; Martinian, Lillian; Scheffer, Ingrid E.; Thom, Maria; Sisodiya, Sanjay M.

MFN2 mutations cause severe phenotypes in most patients with CMT2A

NEUROLOGY

IF8.5

2011-05-17

166

OAAI

Feely, S. M. E.; Laura, M.; Siskind, C. E.; Sottile, S.; Davis, M.; Gibbons, V. S.; Reilly, M. M.; Shy, M. E.

An Intragenic Duplication in Guanosine Triphosphate Cyclohydrolase-1 Gene in a Dopa-Responsive Dystonia Family

MOVEMENT DISORDERS

IF7.6

2011-02-01

PREAI

Ling, Helen; Polke, James M.; Sweeney, Mary G.; Haworth, Andrea; Sandford, Catherine A.; Heales, Simon J. R.; Wood, Nicholas W.; Davis, Mary B.; Lees, Andrew J.

研究方向