Here are the links to the above dates from PedsCases Notes:
Malaria
Published: Mar 09, 2025
This PedsCases note provides a one-page overview on pediatric malaria and its identification and management in Canada. It was created by Tina Madani Kia, a medical student at the University of Alberta with the help of Dr. Qaasim Mian, a pediatrician at the University of Alberta and Dr. Michael Hawkes, a pediatric infectious disease physician at the University of British Columbia.
Published: Feb 15, 2025
This PedsCases Note provides a one-page infographic on Toddler’s Diarrhea. Toddler’s diarrhea is characertized as benign chornic diarrhea in a well appearing toddler. It was created by Julia Craig with the help of Dr. Carrie Lewis
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Published: Feb 10, 2025
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
