Urinary tract infection caused by extended‐spectrum β‐lactamase‐producing bacteria: Risk factors and antibiotic resistance von Albaramki, Jumana H, Abdelghani, Tariq, Dalaeen, Alaa, Khdair Ahmad, Fareed, Alassaf, Abeer, Odeh, Rasha, Akl, Kamal

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RE: A guideline for the inpatient care of children with pyelonephritis von Akl, Kamal

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Orange-colored diapers in infants from families with gout von Akl, Kamal F.

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Neurological and cardiac complications in a cohort of children with end-stage renal disease von al-Barmaki, Jumanah H., al-Ammuri, Iyad A., Aql, Kamal F.

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Pediatric nephrology practice in Jordan von Aql, Kamal, Hazza, Isa

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The anomalies associated with congenital solitary functioning kidney in children von Aql, Kamal

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Home Made Pneumatic Otoscopy von Akl, Kamal F.

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Neonatal Urinary Tract Infection in a Tertiary Care Center in Amman, Jordan von Jumana Albaramki, Manar Al-lawama, Manar Jarra, Randa Alqaisi, Rama Jadallah, Asma AL-Mustafa, Eman Badran, Kamal Akl

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Macrothrombocytopenia, psychomotor retardation, and nephropathy: a novel familial syndrome von Akl, Kamal F, Qudah, Abdul Karim, Awidi, Abdalla, Suleiman, Mohammad Jaber, Ababneh, Nidaa, Bsoul, Nazzal, Magablah, Ahmad

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Molecular analysis of the CTNS gene in Jordanian families with nephropathic cystinosis von Jaradat, Saied, Al-Rababah, Bothina, Hazza, Issa, Akl, Kamal, Saca, Edward, Al-Younis, Doaa

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Black tongue von Akl, Kamal F

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Acute urine retention induced by ceftriaxone von Aql, Kamal F., Misri, Amirah T., Hjazeen, Maali M.

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Misuse of the wooden tongue depressor von Akl, Kamal F.

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Posterior reversible encephalopathy syndrome von Akl, Kamal F, Samara, Osama A

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Molecular analysis of the CTNS gene in Jordanian families with nephropathic cystinosis von Jaradat, Saied, Al-Rababah, Bothina, Hazza, Issa, Akl, Kamal, Saca, Edward, Al-Younis, Doaa

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Urofacial syndrome von Aql, Kamal, al-Mumani, Hashim M.

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The clinical spectrum of idiopathic hyperuricosuria in children : isolated and associated with hypercalciuria / hyperoxaluria von Aql, Kamal, Ghawanimah, Redab

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Detection of novel LAMA3 mutation in Herlitz junctional epidermolysis bullosa in a Jordanian family von Badran, Eman F., Battah, Hamdi A., Akl, Kamal F, Khalil, Raida W., Al Amori, Iyad

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A family with five siblings affected with nephronophthisis von Wahbah, Ayman, Aql, Kamal, al-Baramki, Jumanah H., Hamid, Radi

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Absent abdominal muscles, nephro-urologic abnormalities, and severe neurologic damage in an infant with 3 chromosomal duplications: A novel syndrome? von Akl, Kamal F., Albaramki, Jumana H., Ghani, Eman A., I. Al Qaisi, Mohammad, Abujaber, Nadeen, Tavares, Purificação

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