S Faisal Ahmed
Biographic Data
| ID | 5221986 |
|---|---|
| NAME | S Faisal Ahmed |
| GIVEN NAMES | S Faisal |
| FAMILY NAME | Ahmed |
| SIGNATURE | AHMED S F |
| AFFILIATIONS | University of Glasgow |
| ORCID | 0000-0003-0689-5549 |
| VERIFIED | Yes |
| TOTAL WORKS | 13 |
| TOTAL CITATIONS | 18 |
| AUTHOR COUNT | 13 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2003 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 1 |
Prevalance of long-Covid-19 syndrome among patients of MMC, Mardan: A descriptive study
Introduction: The COVID-19 is an upper respiratory tract infection caused by the SARS-COV-19 virus. As of 2022, 504M cases have been reported globally with a substantial death toll of 6.2M. Although the conventional symptoms remain the same at the time of onset, the post-recovery symptoms vary. The cause of these divers symptoms and their trigger is still under research. We have conducted this research in order to find out the post-infection sequ…
Electronic Heart (ECG) Monitoring at Birth and Newborn Resuscitation
Background: Approximately 10% of newborns require assistance at delivery, and heart rate (HR) is the primary vital sign providers use to guide resuscitation methods. In 2016, the American Heart Association (AHA) suggested electrocardiogram in the delivery room (DR-ECG) to measure heart rate during resuscitation. This study aimed to compare the frequency of resuscitation methods used before and after implementation of the AHA recommendations. Meth…
Patient-reported experience of clinical care of osteogenesis imperfecta (OI) during the Covid-19 pandemic
Background: Research on the effects of the COVID-19 pandemic on people with rare diseases is limited. Few studies compare healthcare throughout the progression of the ongoing pandemic. Aims: To assess the impact of the pandemic on individuals with osteogenesis imperfecta across two consecutive years, understand what challenges were encountered, and analyse the experience of remote consultation. Methods: An initial survey was distributed following…
The Quality Evaluation of Rare Disease Registries—An Assessment of the Essential Features of a Disease Registry
Rare disease (RD) registries aim to promote data collection and sharing, and facilitate multidisciplinary collaboration with the overall aim of improving patient care. Recommendations relating to the minimum standards necessary to develop and maintain high quality registries are essential to ensure high quality data and sustainability of registries. The aim of this international study was to survey RD registry leaders to ascertain the level of co…
Recommendations for Improving the Quality of Rare Disease Registries
Rare diseases (RD) patient registries are powerful instruments that help develop clinical research, facilitate the planning of appropriate clinical trials, improve patient care, and support healthcare management. They constitute a key information system that supports the activities of European Reference Networks (ERNs) on rare diseases. A rapid proliferation of RD registries has occurred during the last years and there is a need to develop guidan…
Defining and Measuring Community Engagement and Community-Engaged Research: Clinical and Translational Science Institutional Practices
Defining and Measuring Community Engagement and Community-Engaged Research: Clinical and Translational Science Institutional Practices Milton “Mickey” Eder, PhD, Eunbyul Evans, PhD, Melanie Funes, PhD, Hui Hong, Katja Reuter, PhD, Syed Ahmed, MD, MPH, DrPH, Karen Calhoun, Giselle Corbie-Smith, MD, MSc, Gaurav Dave, MD, DrPH, MPH, Mia DeFino, MS, Eileen Harwood, PhD, Anne Kissack, MPH, RD, Lawrence C. Kleinman, MD, MPH, and Nina Wallerstein, DrPH …
The impact of bivalent HPV vaccine on cervical intraepithelial neoplasia by deprivation in Scotland: Reducing the gap
BACKGROUND: Cervical cancer disproportionately affects women from lower socioeconomic backgrounds. A human papillomavirus (HPV) vaccination programme was introduced in Scotland in 2008 with uptake being lower and inequitable in a catch-up cohort run for the first three years of the programme compared with the routine programme. The socioeconomic differences in vaccine uptake have the potential to further increase the inequality gap in regards to …
Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care
The goal of this update regarding the diagnosis and care of persons with disorders of sex development (DSDs) is to address changes in the clinical approach since the 2005 Consensus Conference, since knowledge and viewpoints change. An effort was made to include representatives from a broad perspective including support and advocacy groups. The goal of patient care is focused upon the best possible quality of life (QoL). The field of DSD is contin…
Management of children with disorders of sex development: New care standards explained
Over the last decade, increasing attention has been focused on the health of children with disorders of sex development (DSD) and the gaps in our knowledge of how early care may be linked to long-term outcome. In the current environment of greater collaboration as part of clinical and research networks, stronger links have been forged between professionals, patients and parents and guidelines have been developed for directing care. With continuin…
Declaración de consenso sobre el manejo de desórdenes intersexuales1
HPV vaccine: Positive insights from universal adolescent HepB vaccination
The introduction of universal adolescent HPV vaccination in schools has a positive outlook
Consensus Statement on Management of Intersex Disorders
The birth of an intersex child prompts a long-term management strategy that involves a myriad of professionals working with the family. There has been progress in diagnosis, surgical techniques, understanding psychosocial issues and in recognizing and accepting the place of patient advocacy. The Lawson Wilkins Paediatric Endocrine Society (LWPES) and the European Society for Paediatric Endocrinology (ESPE) considered it timely to review the manag…
Psychological Outcomes and Gender-Related Development in Complete Androgen Insensitivity Syndrome
Psychological Outcomes and Gender-Related Development in Complete Androgen Insensitivity Syndrome
The impact of bivalent HPV vaccine on cervical intraepithelial neoplasia by deprivation in Scotland: Reducing the gap
BACKGROUND: Cervical cancer disproportionately affects women from lower socioeconomic backgrounds. A human papillomavirus (HPV) vaccination programme was introduced in Scotland in 2008 with uptake being lower and inequitable in a catch-up cohort run for the first three years of the programme compared with the routine programme. The socioeconomic differences in vaccine uptake have the potential to further increase the inequality gap in regards to …
HPV vaccine: Positive insights from universal adolescent HepB vaccination
The introduction of universal adolescent HPV vaccination in schools has a positive outlook
Psychological Outcomes and Gender-Related Development in Complete Androgen Insensitivity Syndrome
Consensus Statement on Management of Intersex Disorders
The birth of an intersex child prompts a long-term management strategy that involves a myriad of professionals working with the family. There has been progress in diagnosis, surgical techniques, understanding psychosocial issues and in recognizing and accepting the place of patient advocacy. The Lawson Wilkins Paediatric Endocrine Society (LWPES) and the European Society for Paediatric Endocrinology (ESPE) considered it timely to review the manag…
HPV vaccine: Positive insights from universal adolescent HepB vaccination
The introduction of universal adolescent HPV vaccination in schools has a positive outlook
Management of children with disorders of sex development: New care standards explained
Over the last decade, increasing attention has been focused on the health of children with disorders of sex development (DSD) and the gaps in our knowledge of how early care may be linked to long-term outcome. In the current environment of greater collaboration as part of clinical and research networks, stronger links have been forged between professionals, patients and parents and guidelines have been developed for directing care. With continuin…
Declaración de consenso sobre el manejo de desórdenes intersexuales1
Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care
The goal of this update regarding the diagnosis and care of persons with disorders of sex development (DSDs) is to address changes in the clinical approach since the 2005 Consensus Conference, since knowledge and viewpoints change. An effort was made to include representatives from a broad perspective including support and advocacy groups. The goal of patient care is focused upon the best possible quality of life (QoL). The field of DSD is contin…
The impact of bivalent HPV vaccine on cervical intraepithelial neoplasia by deprivation in Scotland: Reducing the gap
BACKGROUND: Cervical cancer disproportionately affects women from lower socioeconomic backgrounds. A human papillomavirus (HPV) vaccination programme was introduced in Scotland in 2008 with uptake being lower and inequitable in a catch-up cohort run for the first three years of the programme compared with the routine programme. The socioeconomic differences in vaccine uptake have the potential to further increase the inequality gap in regards to …
Recommendations for Improving the Quality of Rare Disease Registries
Rare diseases (RD) patient registries are powerful instruments that help develop clinical research, facilitate the planning of appropriate clinical trials, improve patient care, and support healthcare management. They constitute a key information system that supports the activities of European Reference Networks (ERNs) on rare diseases. A rapid proliferation of RD registries has occurred during the last years and there is a need to develop guidan…
Defining and Measuring Community Engagement and Community-Engaged Research: Clinical and Translational Science Institutional Practices
Defining and Measuring Community Engagement and Community-Engaged Research: Clinical and Translational Science Institutional Practices Milton “Mickey” Eder, PhD, Eunbyul Evans, PhD, Melanie Funes, PhD, Hui Hong, Katja Reuter, PhD, Syed Ahmed, MD, MPH, DrPH, Karen Calhoun, Giselle Corbie-Smith, MD, MSc, Gaurav Dave, MD, DrPH, MPH, Mia DeFino, MS, Eileen Harwood, PhD, Anne Kissack, MPH, RD, Lawrence C. Kleinman, MD, MPH, and Nina Wallerstein, DrPH …
The Quality Evaluation of Rare Disease Registries—An Assessment of the Essential Features of a Disease Registry
Rare disease (RD) registries aim to promote data collection and sharing, and facilitate multidisciplinary collaboration with the overall aim of improving patient care. Recommendations relating to the minimum standards necessary to develop and maintain high quality registries are essential to ensure high quality data and sustainability of registries. The aim of this international study was to survey RD registry leaders to ascertain the level of co…
Patient-reported experience of clinical care of osteogenesis imperfecta (OI) during the Covid-19 pandemic
Background: Research on the effects of the COVID-19 pandemic on people with rare diseases is limited. Few studies compare healthcare throughout the progression of the ongoing pandemic. Aims: To assess the impact of the pandemic on individuals with osteogenesis imperfecta across two consecutive years, understand what challenges were encountered, and analyse the experience of remote consultation. Methods: An initial survey was distributed following…
Prevalance of long-Covid-19 syndrome among patients of MMC, Mardan: A descriptive study
Introduction: The COVID-19 is an upper respiratory tract infection caused by the SARS-COV-19 virus. As of 2022, 504M cases have been reported globally with a substantial death toll of 6.2M. Although the conventional symptoms remain the same at the time of onset, the post-recovery symptoms vary. The cause of these divers symptoms and their trigger is still under research. We have conducted this research in order to find out the post-infection sequ…
Electronic Heart (ECG) Monitoring at Birth and Newborn Resuscitation
Background: Approximately 10% of newborns require assistance at delivery, and heart rate (HR) is the primary vital sign providers use to guide resuscitation methods. In 2016, the American Heart Association (AHA) suggested electrocardiogram in the delivery room (DR-ECG) to measure heart rate during resuscitation. This study aimed to compare the frequency of resuscitation methods used before and after implementation of the AHA recommendations. Meth…
Medicine (11 works) · Sexual Differentiation and Disorders (5 works) · Family medicine (4 works) · Computer Science (3 works) · Developmental psychology (3 works) · Disease (3 works) · Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 works) · Health care (3 works) · Internal Medicine (3 works) · Psychiatry (3 works)