Cystic Fibrosis: Is it Extremely Rare or Invariably Missed? An Observational Study in Bangladesh Scenario
Keywords:
cystic fibrosis, sweat chloride, pilocarpine iontophoresis, bangladesh
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V Zvereff, H Faruki, M Edwards, K Friedman (2013) Cystic fibrosis carrier screening in a North American population. 16(7), 539-546.
B Karem, J Rommens, J Bichnan (1989) Idetification of cystic fibrosis gene. 245, 1673-1680.
Raymond Frizzell (1995) Functions of the Cystic Fibrosis Transmembrane Conductance Regulator Protein. 151(3_pt_2), S54-S58.
Beryl Rosenstein, Terry Langbaum (1987) Misdiagnosis of Cystic Fibrosis. 26(2), 78-82.
V Legrys (1996) Sweat testing for the diagnosis of cystic fibrosis: Practical considerations. 129, 892-897.
Jake Collie, R Massie, Oliver Jones, Vicky Legrys, Ronda Greaves (2014) Sixty-five years since the New York heat wave: Advances in sweat testing for cystic fibrosis. 49(2), 106-117.
Pamela Devis (2008) Cystic Fibrosis since 1938. 173, 477-482.
J Dodge, S Morison, P Lewis, E Coles, D Geddes, G Russel (1997) Incidence, population and survival of cystic fibrosis in UK 1968-95. UKCF Survey Management Committee. 77, 493-496.
Ada Hamosh, Stacey Fitzsimmons, Milan Macek, Michael Knowles, Beryl Rosenstein, Garry Cutting (1998) Comparison of the clinical manifestations of cystic fibrosis in black and white patients. 132(2), 255-259.
S Kabra, M Kabra, R Lodha, S Shastri (2007) Cystic fibrosis in India. 42(12), 1087-1094.
S Kabra, M Kabra, S Gera, R Lodha, K Sreedevi, S Chacko (2002) An indigenously developed method for sweat collection and estimation of chloride for diagnosis of cystic fibrosis. 39, 1039-1043.
Lewis Gibson, Robert Cooke (1959) A TEST FOR CONCENTRATION OF ELECTROLYTES IN SWEAT IN CYSTIC FIBROSIS OF THE PANCREAS UTILIZING PILOCARPINE BY IONTOPHORESIS. 23(3), 545-549.
O Schales, S Schales (1941) A simple and accurate method for determination of chloride in biological fluids. 140, 879-884.
Philip Farrell, Terry White, Clement Ren, Sarah Hempstead, Frank Accurso, Nico Derichs, Michelle Howenstine, Susanna Mccolley, Michael Rock, Margaret Rosenfeld, Isabelle Sermet-Gaudelus, Kevin Southern, Bruce Marshall, Patrick Sosnay (2017) Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation. 181, S4-S15.e1.
Arm Kabir, Sudipta Roy, Rahat Habib, Kazi Anwar, Md. Mollah, Ruhul Amin, Al Mridha, Jasim Majumder, Md. Hossain, Nazmul Haque, Shakil Ahmed, Mohammod Chisti (2020) Cystic Fibrosis Diagnosed Using Indigenously Wrapped Sweating Technique: First Large-Scale Study Reporting Socio-Demographic, Clinical, and Laboratory Features among the Children in Bangladesh A Lower Middle Income Country. 7, 1-15.
Clsi (2009) Sweat Testing: Sample Collection and Quantitative Chloride Analysis; Approved Guideline -Third Edition.
M Philip, J Beryl (2008) Guidelines for diagnosis of cystic fibrosis in new borns through older adults: Cystic Fibrosis Foundation Consensus Report. 53, 4-S14.
S Kabra, M Kabra, R Lodha, S Shastri, S Ghosh, R Pandey (2003) Clinical profile and frequency of delta f508 mutation in Indian children in Cystic Fibrosis. 40, 612-619.
Manzoor Raina, M Khan, S Malik, Abh Raina, J Makhdoomi (2018) Assessment of Correlation between Sweat Chloride Levels and Clinical Features of Cystic Fibrosis Patients. 10(12), C01-C6.
Masarat Kawoosa, Mushtaq Bhat, Syed Ali, Imran Hafeez, Shivram Shastri (2014) Clinical and mutation profile of children with cystic fibrosis in Jammu and Kashmir. 51(3), 185-189.
Meenu Singh, Rajendra Prasad, Lata Kumar (2002) Cystic fibrosis in north Indian children. 69(7), 627-629.
Fitz Simmons (1993) The changing epidemiology of cystic fibrosis. 122, 1-9.
Al Mahroos, F (1998) Cystic fibrosis in Bahrain incidence, phenotype and outcome. 44(1), 35-39.
Marie Desgeorges, André Mégarbané, Caroline Guittard, Soukeyna Carles, Jacques Loiselet, Jacques Demaille, M Claustres (1997) Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities. 100(2), 279-283.
M Mona, Walaa El-Falaki, Shahin, R Noussa, Aliaa El-Basha, Dina Ali, Mona Mehaney, El-Attai (2014) Profile of cystic fibrosis in a single referral centre in Egypt. 5(5), 563-568.
F Farahmand, M Khalili, L Shahbaznejad, A Hibrod-Mobarakeh, M Sani, A Khodad (2013) Clinical presentation cystic fibrosis at the time of diagnosis: a multicenter study in a region without new born screening. 24(6), 541-545.
U Shah, T Moatter, Z Bhutta (2006) Profile and factors determining outcome in a cohort of cystic fibrosis patients seen at Aga Khan university hospital, Karachi, Pakistan. 52, 132-135.
D Aziz, A Billo, A Qureshi, M Khalid, S Kirmani (2017) Clinical and laboratory profile of cystic fibrosis: Experience of a tertiary care Centre in Pakistan. 33(3), 554-549.
Neluwa Indika, Dinesha Vidanapathirana, Hewa Dilanthi, Grace Kularatnam, Nambage Chandrasiri, Eresha Jasinge (2019) Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka. 20(1), 89.
I Bowler, E Estlin, J Littlewood (1999) Cystic Fibrosis in Asians. 122, 1-9.
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2022-07-15
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