Insulin pump therapy during Ramadan fasting in type 1 diabetic adolescents

Por Bin-Abbas, Bassam Saleh
Publicado no Ann Saudi Med (2008)

Knowledge, awareness, attitudes and sources of vitamin D deficiency and sufficiency in Saudi children

Por Alshamsan, Fatimah M., Bin-Abbas, Bassam S.
Publicado no Saudi Med J (2016)

Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?

Por Mustafa, Manal, Moghrabi, Nabil, Bin-Abbas, Bassam
Publicado no Case Rep Endocrinol (2014)

Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Por Bin-Abbas, Bassam S., Sakati, Nadia A., Al-Ashwal, Abdullah A.
Publicado no Ann Saudi Med (2006)

Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency

Por Bin-Abbas, Bassam S., Sakati, Nadia A., Al-Ashwal, Abdullah A.
Publicado no Ann Saudi Med (2006)

Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Por Bin-Abbas, Bassam S., Sakati, Nadia A., Al-Ashwal, Abdullah A.
Publicado no Ann Saudi Med (2006)

Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients

Por Adi, Ahmad, Bin Abbas, Bassam, Al Hamed, Mohamed, Al Tassan, Nada, Bakheet, Dana
Publicado no Genes (Basel) (2015)

Effect of Mobile Phone Short Text Messages on Glycemic Control in Type 2 Diabetes

Por Bin Abbas, Bassam, Al Fares, Abdullah, Jabbari, Musleh, El Dali, Abdelmoneim, Al Orifi, Fahad
Publicado no Int J Endocrinol Metab (2015)

Two novel LHX3 mutations in patients with combined pituitary hormone deficiency including cervical rigidity and sensorineural hearing loss

Por Ramzan, Khushnooda, Bin-Abbas, Bassam, Al-Jomaa, Lolwa, Allam, Rabab, Al-Owain, Mohammed, Imtiaz, Faiqa
Publicado no BMC Endocr Disord (2017)

Decline in menarcheal age among Saudi girls

Por Alwan, Ibrahim A. Al, Ibrahim, Areej A., Badri, Motasim A., Dubayee, Mohammed S. Al, Bin-Abbas, Bassam S.
Publicado no Saudi Med J (2015)

Selenium Supplementation Fails to Correct the Selenoprotein Synthesis Defect in Subjects with SBP2 Gene Mutations

Por Schomburg, Lutz, Dumitrescu, Alexandra M., Liao, Xiao-Hui, Bin-Abbas, Bassam, Hoeflich, Johanna, Köhrle, Josef, Refetoff, Samuel
Publicado em 2009

Heterogeneity in Phenotype of Usher-Congenital Hyperinsulinism Syndrome: Hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conv...

Por Al Mutair, Angham N., Brusgaard, Klaus, Bin-Abbas, Bassam, Hussain, Khalid, Felimban, Naila, Al Shaikh, Adnan, Christesen, Henrik T.
Publicado em 2013