Geometric control of vascular networks to enhance engineered tissue integration and function von Baranski, Jan D., Chaturvedi, Ritika R., Stevens, Kelly R., Eyckmans, Jeroen, Carvalho, Brian, Solorzano, Ricardo D., Yang, Michael T., Miller, Jordan S., Bhatia, Sangeeta N., Chen, Christopher S.

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The oxytocin system in patients with craniopharyngioma: A systematic review von Mann, Amy, Kalitsi, Jennifer, Jani, Khushali, Martins, Daniel, Kapoor, Ritika R, Paloyelis, Yannis

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American Life in Realtime: a benchmark registry of health data for equitable precision health von Chaturvedi, Ritika R., Angrisani, Marco, Troxel, Wendy M., Gutsche, Tania, Ortega, Eva, Jain, Monika, Boch, Adrien, Kapteyn, Arie

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Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management von Gϋemes, Maria, Rahman, Sofia Asim, Kapoor, Ritika R., Flanagan, Sarah, Houghton, Jayne A. L., Misra, Shivani, Oliver, Nick, Dattani, Mehul Tulsidas, Shah, Pratik

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The emerging role of disease-associated microglia in Parkinson's disease von Samant, Ritika R, Standaert, David G, Harms, Ashley S

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A sensor-enabled cloud-based computing platform for computational brain biomechanics von Menghani, Ritika R., Das, Anil, Kraft, Reuben H.

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A case of thyroid storm in a child associated with transient central diabetes insipidus von Agrawal, Pankaj, Kapoor, Ritika R, Buchanan, Charles, Arya, Ved Bhushan

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Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism von Kapoor, Ritika R, Flanagan, Sarah E, Arya, Ved Bhushan, Shield, Julian P, Ellard, Sian, Hussain, Khalid

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Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389 von Yau, Daphne, Laver, Thomas W, Dastamani, Antonia, Senniappan, Senthil, Houghton, Jayne A L, Shaikh, Guftar, Cheetham, Tim, Mushtaq, Talat, Kapoor, Ritika R, Randell, Tabitha, Ellard, Sian, Shah, Pratik, Banerjee, Indraneel, Flanagan, Sarah E

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Autoimmune Encephalitis and Autism Spectrum Disorder von Whiteley, Paul, Marlow, Ben, Kapoor, Ritika R, Blagojevic-Stokic, Natasa, Sala, Regina

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Mycobacterium leprae in Nine-Banded Armadillos (Dasypus novemcinctus), Ecuador von Romero-Alvarez, Daniel, Calvopiña, Manuel, Cisneros-Vásquez, Emily, Garzon-Chavez, Daniel, Warren, Alaine K, Bennett, Lauren S, Janapati, Ritika R, Bastidas-Caldes, Carlos, Cabezas-Moreno, Melanie, de Waard, Jacobus H, Silva-Martinod, Daniela, Schaub, Roxane, Jackson, Mary, Peterson, A Townsend, Avanzi, Charlotte

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Embedded Finite Elements for Modeling Axonal Injury von Garimella, Harsha T., Menghani, Ritika R., Gerber, Jesse I., Sridhar, Srikumar, Kraft, Reuben H.

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Hyperinsulinaemic hypoglycaemia in deoxyguanosine kinase deficiency von Arya, Ved Bhushan, Dhawan, Anil, Kapoor, Ritika R.

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Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review von Mann, Amy, Aghababaie, Arameh, Kalitsi, Jennifer, Martins, Daniel, Paloyelis, Yannis, Kapoor, Ritika R

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Transient neonatal hyperinsulinaemic hypoglycaemia: perinatal predictors of length and cost of stay von Kozen, Kazune, Dassios, Theodore, Kametas, Nick, Kapoor, Ritika R., Greenough, Anne

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Low‐dose diazoxide therapy in hyperinsulinaemic hypoglycaemia von Ng, Amy Yi‐Lin, Agrawal, Pankaj, Vijayan, Roopa, Arya, Ved B., Kapoor, Ritika R., Shah, Pratik

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Prolactinoma in childhood and adolescence—Tumour size at presentation predicts management strategy: Single centre series and a systematic review and meta‐analysis von Arya, Ved Bhushan, Aylwin, Simon J. B., Hulse, Tony, Ajzensztejn, Michal, Kalitsi, Jennifer, Kalogirou, Nicolas, Bodi, Istvan, Thomas, Nick, Hampton, Tim, Kapoor, Ritika R., Buchanan, Charles R.

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Advances in the diagnosis and management of hyperinsulinemic hypoglycemia von Kapoor, Ritika R, James, Chela, Hussain, Khalid

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Xq27.1 Duplication Encompassing SOX3: Variable Phenotype and Smallest Duplication Associated with Hypopituitarism to Date – A Large Case Series of Unrelated Patients and a Literatu... von Arya, Ved Bhushan, Chawla, Garima, Nambisan, Aparna K.R., Muhi-Iddin, Nadia, Vamvakiti, Ekaterini, Ajzensztejn, Michal, Hulse, Tony, Ferreira Pinto, Clare, Lahiri, Nayana, Bint, Susan, Buchanan, Charles R., Kapoor, Ritika R.

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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or... von Edghill, Emma L, Flanagan, Sarah E, Patch, Ann-Marie, Boustred, Chris, Parrish, Andrew, Shields, Beverley, Shepherd, Maggie H, Hussain, Khalid, Kapoor, Ritika R, Malecki, Maciej, MacDonald, Michael J, Støy, Julie, Steiner, Donald F, Philipson, Louis H, Bell, Graeme I, Hattersley, Andrew T, Ellard, Sian

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