CLINICO-EPIDEMIOLOGICAL FEATURES OF HYPERTENSIVE SUBJECTS IN KASSALA TOWN, EASTERN SUDAN

por Osman, El Fadil M., Suleiman, Ikhlas, Alzubair, Ahmed G.
Publicado 2007

Disorders of the calcium-sensing receptor and partner proteins: insights into the molecular basis of calcium homeostasis

por Hannan, Fadil M, Babinsky, Valerie N, Thakker, Rajesh V
Publicado 2016

Autosomal Dominant Hypocalcemia Type 1 (ADH1) Associated With Myoclonus and Intracerebral Calcifications

por Elston, Marianne S, Elajnaf, Taha, Hannan, Fadil M, Thakker, Rajesh V
Publicado 2022

Genetics of Monogenic Disorders of Calcium and Bone Metabolism

por Newey, Paul J, Hannan, Fadil M., Wilson, Abbie, Thakker, Rajesh V
Publicado 2022

Hypercalcemic Disorders in Children

por Stokes, Victoria J, Nielsen, Morten F, Hannan, Fadil M, Thakker, Rajesh V
Publicado 2017

Genetic approaches to metabolic bone diseases

por Hannan, Fadil M., Newey, Paul J., Whyte, Michael P., Thakker, Rajesh V.
Publicado 2018

Genome-wide screening of lectin putative genes from Sorghum bicolor L., distribution in QTLs and a probable implications of lectins in abiotic stress tolerance

por Osman, Makarim El-fadil M., Dirar, Amina Ibrahim, Konozy, Emadeldin Hassan E.
Publicado 2022

On the fuel cycle and neutron fluxes of the high flux reactor at ILL Grenoble

por Ridikas, D, Fioni, G, Goberis, P, Déruelle, O, Fadil, M, Marie, F, Röttger, S
Publicado 2000

The striking mimics between COVID-19 and malaria: A review

por Konozy, Emadeldin Hassan E., Osman, Makarim El-fadil M., Ghartey-Kwansah, George, Abushama, Hind Mohamed
Publicado 2022

Association Studies of Calcium-Sensing Receptor (CaSR) Polymorphisms with Serum Concentrations of Glucose and Phosphate, and Vascular Calcification in Renal Transplant Recipients

por Babinsky, Valerie N., Hannan, Fadil M., Youhanna, Sonia C., Maréchal, Céline, Jadoul, Michel, Devuyst, Olivier, Thakker, Rajesh V.
Publicado 2015

A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

por Gorvin, Caroline M, Cranston, Treena, Hannan, Fadil M, Rust, Nigel, Qureshi, Asjid, Nesbit, M Andrew, Thakker, Rajesh V
Publicado 2016

Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss‐of‐Function Gα(11) Mutation

por Gorvin, Caroline M, Hannan, Fadil M, Cranston, Treena, Valta, Helena, Makitie, Outi, Schalin‐Jantti, Camilla, Thakker, Rajesh V
Publicado 2017

Role of Ca(2+) and L-Phe in Regulating Functional Cooperativity of Disease-Associated “Toggle” Calcium-Sensing Receptor Mutations

por Zhang, Chen, Mulpuri, Nagaraju, Hannan, Fadil M., Nesbit, M. Andrew, Thakker, Rajesh V., Hamelberg, Donald, Brown, Edward M., Yang, Jenny J.
Publicado 2014

Calcium-sensing receptor residues with loss- and gain-of-function mutations are located in regions of conformational change and cause signalling bias

por Gorvin, Caroline M, Frost, Morten, Malinauskas, Tomas, Cranston, Treena, Boon, Hannah, Siebold, Christian, Jones, E Yvonne, Hannan, Fadil M, Thakker, Rajesh V
Publicado 2018

Protocol for an observational study investigating hormones triggering the onset of sustained lactation: the INSIGHT study

por Rostom, Hussam, Meng, Xin, Price, Helen, Fry, Alexandria, Elajnaf, Taha, Humphrey, Robert, Guha, Nishan, James, Tim, Kennedy, Stephen H, Hannan, Fadil M
Publicado 2022

Neonatal Hypocalcemic Seizures in Offspring of a Mother With Familial Hypocalciuric Hypercalcemia Type 1 (FHH1)

por Dharmaraj, Poonam, Gorvin, Caroline M, Soni, Astha, Nelhans, Nick D, Olesen, Mie K, Boon, Hannah, Cranston, Treena, Thakker, Rajesh V, Hannan, Fadil M
Publicado 2020

SAT-404 Neonatal Hypocalcemic Seizures in Offspring of a Mother with Familial Hypocalciuric Hypercalcemia Type 1 (FHH1)

por Hannan, Fadil M, Dharmaraj, Poonam, Gorvin, Caroline M, Soni, Astha, Nelhans, Nick D, Olesen, Mie Kronborg, Boon, Hannah, Cranston, Treena, Thakker, Rajesh V
Publicado 2020

Spectrum of germline AIRE mutations causing APS-1 and familial hypoparathyroidism

por Cranston, Treena, Boon, Hannah, Olesen, Mie K, Ryan, Fiona J, Shears, Deborah, London, Rosemary, Rostom, Hussam, Elajnaf, Taha, Thakker, Rajesh V, Hannan, Fadil M
Publicado 2022

Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population

por Dershem, Ridge, Gorvin, Caroline M., Metpally, Raghu P.R., Krishnamurthy, Sarathbabu, Smelser, Diane T., Hannan, Fadil M., Carey, David J., Thakker, Rajesh V., Breitwieser, Gerda E.
Publicado 2020

Calcilytic NPSP795 Increases Plasma Calcium and PTH in an Autosomal Dominant Hypocalcemia Type 1 Mouse Model

por Hannan, Fadil M, Gorvin, Caroline M, Babinsky, Valerie N, Olesen, Mie K, Stewart, Michelle, Wells, Sara, Cox, Roger D, Nemeth, Edward F, Thakker, Rajesh V
Publicado 2020