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Serum Magnesium and Vitamin D Levels as Indicators of Asthma Severity
Serum Magnesium and Vitamin D Levels as Indicators of Asthma Severity
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Serum Magnesium and Vitamin D Levels as Indicators of Asthma Severity

Shaikh, Mohammed Nadeem ; Malapati, Brahma Reddy ; Gokani, Ruchi ; Patel, Bhavita ; Chatriwala, Mitul Sandford, Andrew ; Andrew Sandford

Pulmonary Medicine, 2016-01, Vol.2016, p.1643717-5 [Periódico revisado por pares]

Egypt: Hindawi Limiteds

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2
Sequencing Alpha-1 MZ Individuals Shows Frequent Biallelic Mutations
Sequencing Alpha-1 MZ Individuals Shows Frequent Biallelic Mutations
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Sequencing Alpha-1 MZ Individuals Shows Frequent Biallelic Mutations

Foil, Kimberly E. ; Blanton, M. Gwen ; Sanders, Chris ; Kim, Joannah ; Al Ashry, Haitham S. ; Kumbhare, Suchit ; Strange, Charlie Sandford, Andrew ; Andrew Sandford

Pulmonary medicine, 2018-01, Vol.2018, p.2836389-6 [Periódico revisado por pares]

Egypt: Hindawi

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3
The Interpretation of Dyspnea in the Patient with Asthma
The Interpretation of Dyspnea in the Patient with Asthma
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The Interpretation of Dyspnea in the Patient with Asthma

Lavietes, Marc H. Sandford, Andrew ; Andrew Sandford

Pulmonary Medicine, 2015-01, Vol.2015, p.869673-4 [Periódico revisado por pares]

Egypt: Hindawi Limiteds

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4
Radiation Induced DNA Damage in Operators Performing Endovascular Aortic Repair
Radiation Induced DNA Damage in Operators Performing Endovascular Aortic Repair
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Radiation Induced DNA Damage in Operators Performing Endovascular Aortic Repair

El-Sayed, Tamer ; Patel, Ashish S ; Cho, Jun S ; Kelly, James A ; Ludwinski, Francesca E ; Saha, Prakash ; Lyons, Oliver T ; Smith, Alberto ; Modarai, Bijan

Circulation (New York, N.Y.), 2017-12, Vol.136 (25), p.2406-2416 [Periódico revisado por pares]

United States: by the American College of Cardiology Foundation and the American Heart Association, Inc

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5
Prevalence and architecture of de novo mutations in developmental disorders
Prevalence and architecture of de novo mutations in developmental disorders
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Prevalence and architecture of de novo mutations in developmental disorders

McRae, Jeremy F ; Clayton, Stephen ; Mason, Laura E ; Tivey, Adrian R ; Ahmed, Munaza ; Awada, Jana ; Balasubramanian, Meena ; Banka, Siddharth ; Bennett, Chris ; Bernhard, Birgitta ; Bevan, A. Paul ; Blair, Edward ; Blyth, Moira ; Burn, John ; Castle, Bruce ; Clasper, Susan ; Collins, Amanda ; Collinson, Morag N ; Dabir, Tabib ; Davidson, Rosemarie ; Davies, Sally ; Dean, John ; Donnai, Dian ; Ellard, Sian ; Ellis, Ian ; Everest, Sarah ; Foulds, Nicola ; Fryer, Alan ; Gaunt, Lorraine ; Goudie, David ; Gray, Emma ; Greene, Philip ; Gribble, Susan ; Henderson, Alex ; Hildyard, Lucy ; Holden, Simon ; Holder, Muriel ; Ingram, Stuart ; Jackson, Andrew ; Kaemba, Beckie ; Kazembe, Sandra ; Kinning, Esther ; Kraus, Alison ; Kumar, V. K. Ajith ; Lachlan, Katherine ; Lam, Wayne ; Lim, Derek ; Longman, Cheryl ; Lynch, Sally A ; Maher, Eddy ; Maye, Una ; McKay, Kirsten ; McWilliam, Catherine ; Metcalfe, Kay ; Morgan, Sian ; Murday, Victoria ; Murphy, Helen ; Nemeth, Andrea ; Nevitt, Louise ; Newbury-Ecob, Ruth ; Park, Soo-Mi ; Paterson, Joan ; Payne, Stewart ; Perrett, Daniel ; Pratt, Norman ; Quarrell, Oliver ; Randall, Josh ; Rankin, Julia ; Raymond, Lucy ; Robert, Leema ; Roberts, Paul ; Saggar, Anand ; Samant, Shalaka ; Sampson, Julian ; Sandford, Richard ; Selby, Ann ; Sequeira, Cheryl ; Shearing, Emma ; Smith, Audrey ; Smith, Kath ; Splitt, Miranda ; Suri, Mohnish ; Sutton, Vivienne ; Tatton-Brown, Kate ; Temple, I. Karen ; Turner, Claire ; Varghese, Vinod ; Vasudevan, Pradeep ; Vogt, Julie ; Wakeling, Emma ; Wilcox, Sarah ; Williams, Denise ; Williams, Nicola ; Wilson, Louise ; Wright, Michael ; Yates, Laura ; Yau, Michael ; Wright, Caroline F ; FitzPatrick, David R ; Barrett, Jeffrey C

Nature (London), 2017-02, Vol.542 (7642), p.433-438 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Analysis of data from the ERA-EDTA Registry indicates that conventional treatments for chronic kidney disease do not reduce the need for renal replacement therapy in autosomal dominant polycystic kidney disease
Analysis of data from the ERA-EDTA Registry indicates that conventional treatments for chronic kidney disease do not reduce the need for renal replacement therapy in autosomal dominant polycystic kidney disease
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Analysis of data from the ERA-EDTA Registry indicates that conventional treatments for chronic kidney disease do not reduce the need for renal replacement therapy in autosomal dominant polycystic kidney disease

Spithoven, Edwin M. ; Kramer, Anneke ; Meijer, Esther ; Orskov, Bjarne ; Wanner, Christoph ; Caskey, Fergus ; Collart, Frederic ; Finne, Patrik ; Fogarty, Damian G. ; Groothoff, Jaap W. ; Hoitsma, Andries ; Nogier, Marie-Béatrice ; Postorino, Maurizio ; Ravani, Pietro ; Zurriaga, Oscar ; Jager, Kitty J. ; Gansevoort, Ron T. ; on behalf of the ERA-EDTA Registry, the EuroCYST consortium and the WGIKD

Kidney international, 2014-12, Vol.86 (6), p.1244-1252 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension
Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension
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Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

Hadinnapola, Charaka ; Bleda, Marta ; Haimel, Matthias ; Screaton, Nicholas ; Swift, Andrew ; Dorfmüller, Peter ; Preston, Stephen D ; Southwood, Mark ; Hernandez-Sanchez, Jules ; Martin, Jennifer ; Treacy, Carmen ; Yates, Katherine ; Bogaard, Harm ; Church, Colin ; Coghlan, Gerry ; Condliffe, Robin ; Corris, Paul A ; Gibbs, Simon ; Girerd, Barbara ; Holden, Simon ; Humbert, Marc ; Kiely, David G ; Lawrie, Allan ; Machado, Rajiv ; MacKenzie Ross, Robert ; Moledina, Shahin ; Montani, David ; Newnham, Michael ; Peacock, Andrew ; Pepke-Zaba, Joanna ; Rayner-Matthews, Paula ; Shamardina, Olga ; Soubrier, Florent ; Southgate, Laura ; Suntharalingam, Jay ; Toshner, Mark ; Trembath, Richard ; Vonk Noordegraaf, Anton ; Wilkins, Martin R ; Wort, Stephen J ; Wharton, John ; Gräf, Stefan ; Morrell, Nicholas W

Circulation (New York, N.Y.), 2017-11, Vol.136 (21), p.2022-2033 [Periódico revisado por pares]

United States: American Heart Association

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8
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

West, Hannah ; Carss, Keren ; Shakeel, Hassan ; Adlard, Julian ; Cole, Trevor ; Kwong, Ava ; Paterson, Joan ; Searle, Claire ; Skytte, Anne-Bine ; Aitman, Timothy ; Ambegaonkar, Gautum ; Antrobus, Richard ; Arno, Gavin ; Astle, William ; Attwood, Antony ; Austin, Steve ; Bakchoul, Tamam ; Bennett, David ; Bitner-Glindzicz, Maria ; Bleda, Marta ; Bolton-Maggs, Paula ; Booth, Claire ; Clements-Brod, Naomi ; Clowes, Virginia ; Collins, Peter ; Cookson, Victoria ; Creaser-Myers, Amanda ; DaCosta, Rosa ; Davies, Sophie ; Deegan, Patrick ; Dewhurst, Eleanor ; Doffinger, Rainer ; Drewe, Elizabeth ; Favier, Remi ; Firth, Helen ; Furie, Bruce ; Furnell, Abigail ; Gardham, Alice ; Gissen, Paul ; Gomez, Keith ; Graf, Stefan ; Gräf, Stefan ; Greenhalgh, Alan ; Hackett, Scott ; Haimel, Matthias ; Herwadkar, Archana ; Holder, Muriel ; Huissoon, Aarnoud ; James, Roger ; Kennedy, Fiona ; Kingston, Nathalie ; Kuijpers, Taco ; Lawrie, Allan ; Lentaigne, Claire ; Machado, Rajiv ; Maher, Eamonn ; Mangles, Sarah ; Manson, Ania ; Matser, Vera ; McDermott, Elizabeth ; Megy, Karyn ; Millar, Carolyn M. ; Morrell, Nicholas ; Ouwehand, Willem H. ; Papadia, Sofia ; Payne, Jeanette ; Peacock, Andrew ; Pollock, Val ; Quinti, Isabella ; Rayner-Matthews, Paula ; Rehnstrom, Karola ; Rhodes, Christopher J. ; Richardson, Sylvia ; Richter, Alex ; Rondina, Matthew ; Rosser, Elisabeth ; Rue-Albrecht, Kevin ; Sargur, Ravishankar ; Savic, Sinisa ; Schotte, Gwen ; Schulze, Harald ; Seneviratne, Suranjith ; Shamardina, Olga ; Simeoni, Ilenia ; Staines, Simon ; Stark, Hannah ; Stock, Sophie ; Thaventhiran, James ; Thompson, Dorothy ; Toh, Cheng-Hock ; Turek, Wojciech ; Wassmer, Evangeline ; Watt, Christopher ; Wharton, John ; Williamson, Catherine ; Woods, Geoff ; Wort, John ; Yeatman, Nigel ; Tischkowitz, Marc D. ; Maher, Eamonn R.

American journal of human genetics, 2018-07, Vol.103 (1), p.3-18 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration
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Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

Arno, Gavin ; Zihni, Ceniz ; Robson, Anthony G. ; Fiorentino, Alessia ; Black, Graeme ; Ponitkos, Nikos ; Holder, Graham E. ; Aitman, Timothy ; Alachkar, Hana ; Allsup, David ; Anderson, Julie ; Armstrong, Ruth ; Arumugakani, Gururaj ; Ashford, Sofie ; Bakchoul, Tamam ; Bariana, Tadbir K. ; Bibi, Shahnaz ; Bitner-Glindzicz, Maria ; Bolton-Maggs, Paula ; Brady, Angie ; Brown, Matthew ; Caulfield, Mark ; Chitre, Manali ; Clowes, Virginia ; Coghlan, Gerry ; Collins, Peter ; Creaser-Myers, Amanda ; DaCosta, Rosa ; Davies, Sophie ; Deegan, Patrick ; Deshpande, Charu ; Doffinger, Rainer ; Egner, William ; Erwood, Marie ; Favier, Remi ; Flinter, Frances ; Furie, Bruce ; Furnell, Abigail ; Gardham, Alice ; Gattens, Michael ; Ghataorhe, Pavandeep K. ; Gibbs, Simon ; Gilmour, Kimberley ; Gissen, Paul ; Goddard, Sarah ; Gordins, Pavel ; Greinacher, Andreas ; Grigoriadou, Sofia ; Hayman, Grant ; Henderson, Robert ; Henskens, Yvonne ; Holden, Simon ; Hu, Fengyuan ; Jolles, Stephen ; Josifova, Dragana ; Keeling, David ; Kelleher, Peter ; Kelly, Anne M. ; Kuijpers, Taco W. ; Kumararatne, Dinakantha ; Kurian, Manju ; Laffan, Michael A. ; Linger, Rachel ; Machado, Rajiv ; Manson, Ania ; Markus, Hugh S. ; Meehan, Sharon ; Ouwehand, Willem H. ; Park, Soo-Mi ; Parker, Alasdair ; Paterson, Joan ; Peerlinck, Kathelijne ; Perry, David J. ; Qasim, Waseem ; Rankin, Julia ; Rehnstrom, Karola ; Roberts, Irene ; Roughley, Catherine ; Rue-Albrecht, Kevin ; Schulze, Harald ; Shamardina, Olga ; Shipley, Debbie ; Simeoni, Ilenia ; Stephens, Jonathan ; Suntharalingam, Jay ; Thachil, Jecko ; Thaventhiran, James ; Thomas, Ellen ; Titterton, Catherine ; Toh, Cheng-Hock ; Turek, Wojciech ; Turro, Ernest ; Van Geet, Chris ; Wakeling, Emma ; Warner, Timothy Q. ; Webster, Andrew ; Wilkins, Martin ; Young, Tim ; Yu, Ping ; Webster, Andrew R.

American journal of human genetics, 2017-02, Vol.100 (2), p.334-342 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Sensory information processing in patients with nonalcoholic cirrhosis: Short-latency visual, auditory, and somatosensory event-related potentials
Sensory information processing in patients with nonalcoholic cirrhosis: Short-latency visual, auditory, and somatosensory event-related potentials
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Sensory information processing in patients with nonalcoholic cirrhosis: Short-latency visual, auditory, and somatosensory event-related potentials

Sandford, Sandra L. ; Tarter, Ralph E. ; Sclabassi, Robert ; Van Thiel, David H.

Journal of the neurological sciences, 1987-09, Vol.80 (2), p.269-276 [Periódico revisado por pares]

Shannon: Elsevier B.V

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