Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 809 entries
Sorted by: Best Match Show Resources per page
Gender in the Making: Literacies and Identities in Girls' Self-Initiated Making Activities

STEM and girls

Gee E, Parekh P.
GSID: PkU_sYNRblQJ
E Gee, P Parekh - Literacies, Sexualities, and Gender, 2018 - taylorfrancis.com

… In our example, the girls supported each other’s development of capable STEM identities as they engaged in making activities around shared interests. Gee (2000) suggests that affinity …

Using ethnomathematics perspective to widen the vision of mathematics teacher education curriculum

lesson plans

Kasmer L, Naresh N.
GSID: jKLXlBJ4jP0J
N Naresh, L Kasmer - Toward Equity and Social Justice in Mathematics …, 2018 - Springer

In this chapter, we draw upon our collective professional and practical knowledge bases to describe our efforts in fostering connections between ethnomathematics theory and practice …

Non-HIV-associated Kaposi sarcoma in an immunosuppressed melanoma patient treated with dabrafenib.

Journal of clinical pharmacy and therapeutics

Parakh S, Goh M, Andrews MC.
PMID: 26922422
J Clin Pharm Ther. 2016 Jun;41(3):354-356. doi: 10.1111/jcpt.12366. Epub 2016 Feb 28.

WHAT IS KNOWN AND OBJECTIVE: Cutaneous toxicities are commonly seen with BRAF inhibitors, frequently involving painful hyperkeratosis of the feet. We illustrate an unexpected diagnosis of extensive bilateral pedal Kaposi sarcoma masquerading as BRAF inhibitor-related toxicity in a patient...

Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature.

Case reports in pathology

Parekh V, Winokur T, Cerfolio RJ, Stevens TM.
PMID: 27293940
Case Rep Pathol. 2016;2016:6898526. doi: 10.1155/2016/6898526. Epub 2016 May 08.

Adenomatoid tumor is an uncommon benign neoplasm of mesothelial differentiation that distinctively arises in and around the genital organs. In rare instances, it has been described in extragenital locations. There have been only two reports documenting its occurrence in...

Ultrasonic propagation: a technique to reveal field induced structures in magnetic nanofluids.

Ultrasonics

Parekh K, Patel J, Upadhyay RV.
PMID: 25791205
Ultrasonics. 2015 Jul;60:126-32. doi: 10.1016/j.ultras.2015.03.001. Epub 2015 Mar 10.

The paper reports the study of magnetic field induced structures in magnetic nanofluid investigated through ultrasonic wave propagation. Modified Tarapov's theory is used to study variation in velocity anisotropy with magnetic field. The types of field induced structures depend...

Ergonomic T-Handle for Minimally Invasive Surgical Instruments.

Translational medicine @ UniSa

Parekh J, Shepherd D, Hukins D, Maffulli N.
PMID: 27326394
Transl Med UniSa. 2016 May 16;14:38-41. eCollection 2016 May.

A T-handle has been designed to be used for minimally invasive implantation of a dynamic hip screw to repair fractures of the proximal femur. It is capable of being used in two actions: (i) push and hold (while using...

Congenital Hallux Varus with Polydactyly and Syndactyly-Correction in an Adult - A Case Report.

Journal of orthopaedic case reports

Patil SD, Parekh H, Patil VD, Joshi K.
PMID: 27298963
J Orthop Case Rep. 2014 Apr-Jun;4(2):64-8. doi: 10.13107/jocr.2250-0685.171.

INTRODUCTION: Congenital hallux varus of secondary type is associated with polydactyly, syndactyly or other congenital deformities of the foot. Such congenital deformities can be addressed in childhood with soft tissue reconstructive procedures. In adulthood, treatment of these deformities is...

A Rare Case of Progressive Gorham's Disease of Right Shoulder Girdle and Cervical Spine in A Child: 10 Year Follow-up and A Review of Literature.

Journal of orthopaedic case reports

Pn G, Ac D, An P.
PMID: 27299093
J Orthop Case Rep. 2015 Oct-Dec;5(4):30-3. doi: 10.13107/jocr.2250-0685.339.

INTRODUCTION: 'Vanishing Bone Disease' or Gorham's disease is a very rare form of primary idiopathic osteolysis with only around 200 cases being reported till date. We present in this case report a ten year follow-up of a patient who...

Summarizing Simulation Results using Causally-relevant States.

Multi-agent-based simulation ... : International Workshop, MABS ... : revised and invited papers. International Symposium on Military Applications of Blast Simulation

Parikh N, Marathe M, Swarup S.
PMID: 28042620
Multiagent Based Simul. 2016 May;10003:88-103. doi: 10.1007/978-3-319-46840-2_6. Epub 2016 Sep 24.

As increasingly large-scale multiagent simulations are being implemented, new methods are becoming necessary to make sense of the results of these simulations. Even concisely summarizing the results of a given simulation run is a challenge. Here we pose this...

Preservation of Preloaded DMEK Lenticules in Dextran and Non-Dextran-Based Organ Culture Medium.

Journal of ophthalmology

Parekh M, Ruzza A, Ferrari S, Ponzin D.
PMID: 27994884
J Ophthalmol. 2016;2016:5830835. doi: 10.1155/2016/5830835. Epub 2016 Nov 22.

No abstract available.

The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methods.

Canadian journal of kidney health and disease

Samuel S, Scott S, Morgan C, Dart A, Mammen C, Parekh R, Nettel-Aguirre A, Eddy A, Flynn R, Pinsk M, Wade A, Arora S, Benoit G, Bitzan M, Erickson R, Feber J, Filler G, Geier P, Girardin C, Grisaru S, Tee J, Kemp K, Zappitelli M.
PMID: 25960884
Can J Kidney Health Dis. 2014 Jul 22;1:17. doi: 10.1186/2054-3581-1-17. eCollection 2014.

BACKGROUND: Nephrotic syndrome is a commonly acquired kidney disease in children that causes significant morbidity due to recurrent episodes of heavy proteinuria. The management of childhood nephrotic syndrome is known to be highly variable among physicians and care centres.OBJECTIVES:...

Raghib Syndrome Presenting as a Cryptogenic Stroke: Role of Cardiac MRI in Accurate Diagnosis.

Case reports in cardiology

Daruwalla VJ, Parekh K, Tahir H, Collins JD, Carr J.
PMID: 26106490
Case Rep Cardiol. 2015;2015:921247. doi: 10.1155/2015/921247. Epub 2015 May 27.

Raghib Syndrome is a rare developmental complex, which consists of persistence of the left superior vena cava (PLSVC) along with coronary sinus ostial atresia and atrial septal defect. This Raghib complex anomaly has also been associated with other congenital...

Showing 1 to 12 of 809 entries