Common variable immunodeficiency (hypogammaglobulinemia) with an autosomal recessive pattern of inheritance
Lokman, M.N.; George, R.; Sukumaran, S.; Nasuruddin, B.A.
Medical Journal of Malaysia 43(3): 237-242
1988
ISSN/ISBN: 0300-5283 PMID: 3241582 Document Number: 320525
Document emailed within 1 workday
Related Documents
Knoblauch, H.; Urban, M.; Tinschert, S. 1999: Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters Genetic Counseling 10(3): 315-320Temtamy, S.A.; Meligy, R.E.; Osman, N.M.; Meguid, M.S.; Salem, S. 1974: A "new" bone dysplasia with autosomal recessive inheritance Birth Defects Original Article Series 10(10): 165-170
Alvarez-Arratia, M.C.; Muñoz, A.; Martínez Camacho, S.; Buendía Hernández, A.; Attie, F.; Fragoso, R.; García Cruz, D.; Cantú, J.M. 1992: Recessive autosomal inheritance in Marfan syndrome Archivos del Instituto de Cardiologia de Mexico 62(4): 379-382
De Bleecker, J.; De Reuck, J.; Martin, J.J.; Ceuterick, C.; Carton, D.; Leroy, J. 1990: Autosomal recessive inheritance of polymicrogyria and dermatomyositis with paracrystalline inclusions Clinical Neuropathology 9(6): 299-304
Temtamy, S.A.; Shoukry, A.S.; Raafat, M.; Mihareb, S. 1975: Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance Birth Defects Original Article Series 11(2): 104-108
Ferreira, A.; Cohen, L.; Tassan, P.; Pierrot-Deseilligny, C. 1997: Encephalomyelitis secondary to variable common hypogammaglobulinemia Revue Neurologique (Paris) 153(2): 144-145
Avella, A.; Crescenzi, M.; Fiorilli, M. 1988: Diagnostic and therapeutic notes on a case of common variable hypogammaglobulinemia Annali Italiani di Medicina Interna: Organo Ufficiale Della Societa Italiana di Medicina Interna 3(2): 137-140
Solley, G.O.; Dickson, E.R.; Gleich, G.J.; Stobo, J.D. 1979: Chronic active liver disease with common variable hypogammaglobulinemia Mayo Clinic Proceedings 54(2): 127-130
Hockey, A.; Knowles, S.; Davies, D.; Carey, W.; Hurst, J.; Goldblatt, J. 1993: Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance Birth Defects Original Article Series 29(1): 373-382
Maximilian, C.; Ioan, D.M.; Fryns, J.P. 1992: A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype? Genetic Counseling 3(2): 115-118
Roberts, A. 1983: Systems of life no 105. Setting up the systems-5. Diseases with a recessive pattern of inheritance Nursing Times 79(36): 57-60
Morio, T. 2012: Common variable immunodeficiency Nihon Rinsho. Japanese Journal of Clinical Medicine 70(11): 2011-2021
Saiki, O. 1985: Common variable immunodeficiency Rinsho Byori. Japanese Journal of Clinical Pathology 33(11): 1203-1209
Di Gioacchino, M.; Masci, S.; Paolini, F.; Verna, N.; Angelucci, D.; Cavallucci, E.; Paganelli, R. 2002: Common variable immunodeficiency and eosinophilic fasciitis European Journal of Dermatology: Ejd 12(1): 73-74
Blancas-Galicia, L.; Ramírez-Vargas, N.G.; Espinosa-Rosales, F. 2010: Common variable immunodeficiency. a clinical approach Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 62(6): 577-582
Montero Mora, P.; Salas Benítez, H.; Tinajero Castañeda, O.Adriana.; Guidos Fogelbach, G. 2002: Common variable immunodeficiency. Report of 2 cases Revista Alergia Mexico 49(5): 163-165
Astudillo, L.M.; Rigal, F.; Galy-Fourcade, D.; Couret, B.; Arlet-Suau, E. 2002: Osteonecrosis of the knees in a variable common immunodeficiency Clinical and Experimental Rheumatology 20(2): 258
Popa, V. 1988: Lymphocytic interstitial pneumonia of common variable immunodeficiency Annals of Allergy 60(3): 203-206
Ivashkin, V.T.; Kalinin, A.V.; Lapaev, I.B.; Verteletskiĭ, V.V.; Spesivtsev, V.N. 1994: A case of common variable immunodeficiency in monozygotic twins Terapevticheskii Arkhiv 66(2): 56-58
Modrzewska, K.; Wiatr, E.; Langfort, R.; Oniszh, K.; Roszkowski-Sliz, K. 2009: Common variable immunodeficiency in a patient with suspected sarcoidosis Pneumonologia i Alergologia Polska 77(1): 91-96