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Results: 1-25 | 26-29

Table of contents of journal: *Ophthalmic paediatrics and genetics

Results: 1-25/29

Authors: TRABOULSI EI
Citation: Ei. Traboulsi, TO LUMP OR TO SPLIT, Ophthalmic paediatrics and genetics, 14(4), 1993, pp. 141-142

Authors: SMALL KW WEBER J ROSES A PERICAKVANCE P
Citation: Kw. Small et al., NORTH-CAROLINA MACULAR DYSTROPHY (MCDR1) - A REVIEW AND REFINED MAPPING TO 6Q14-Q16.2, Ophthalmic paediatrics and genetics, 14(4), 1993, pp. 143-150

Authors: CHOPDAR A
Citation: A. Chopdar, A VARIANT OF CENTRAL AREOLAR CHOROIDAL DYSTROPHY, Ophthalmic paediatrics and genetics, 14(4), 1993, pp. 151-164

Authors: PETRACCI M PANNINI S FREZZOTTI R
Citation: M. Petracci et al., BUTTERFLY-SHAPED MACULAR DYSTROPHY - LONGITUDINAL CASE-STUDY OF 2 SIBLINGS, Ophthalmic paediatrics and genetics, 14(4), 1993, pp. 165-175

Authors: LORENZ B WORLE J FRIEDL N HASENFRATZ G
Citation: B. Lorenz et al., OCULAR GROWTH IN INFANT APHAKIA - BILATERAL VERSUS UNILATERAL CONGENITAL CATARACTS, Ophthalmic paediatrics and genetics, 14(4), 1993, pp. 177-188

Authors: MACKEY DA
Citation: Da. Mackey, LEBER HEREDITARY OPTIC NEUROPATHY - IS IT A DISEASE OF NORTHERN EUROPE AND ASIA, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 105-107

Authors: OOSTRA RJ BOLHUIS PA BLEEKERWAGEMAKERS EM
Citation: Rj. Oostra et al., MITOCHONDRIAL-DNA ANALYSIS AS A DIAGNOSTIC-TOOL IN SINGLETON CASES OFLEBER HEREDITARY OPTIC NEUROPATHY, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 109-115

Authors: RAJAGOPALAN S RODRIGUES MM WIGGERT B ADVANI SH NAIR CN NICKERSON JM
Citation: S. Rajagopalan et al., RETINOBLASTOMA - INTERPHOTORECEPTOR RETINOID-BINDING PROTEIN MESSENGER-RNA ANALYSIS BY POLYMERASE CHAIN-REACTION, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 117-125

Authors: ABRAMSON DH SENFT SH SERVODIDIO CA ELLSWORTH RM GAMACHE PH
Citation: Dh. Abramson et al., RETINOBLASTOMA AQUEOUS-HUMOR - AROMATIC-AMINO-ACIDS, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 127-130

Authors: LOEWENSTEIN A GODEL V GODEL L LAZAR M
Citation: A. Loewenstein et al., VARIABLE PHENOTYPIC EXPRESSIVITY OF BEST VITELLIFORM DYSTROPHY, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 131-136

Authors: NUSSGENS Z ROGGENKAMPER P
Citation: Z. Nussgens et P. Roggenkamper, LIGNEOUS CONJUNCTIVITIS - 10 YEARS FOLLOW-UP, Ophthalmic paediatrics and genetics, 14(3), 1993, pp. 137-140

Authors: VANLEEUWEN JKW
Citation: Jkw. Vanleeuwen, THE TORCH PASSES ON, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 54-55

Authors: MADREPERLA SA
Citation: Sa. Madreperla, OLIVOPONTOCEREBELLAR ATROPHY WITH RETINAL DEGENERATION - FUNDUS CHARACTERISTICS AND DIAGNOSTIC MRI FINDINGS, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 61-67

Authors: FREZZOTTI R MOTOLESE E BARTOLOMEI A ESPOSTI PE ADDABBO G ROCCHI S FORT A MANFREDI C MASOTTI L TOTI P
Citation: R. Frezzotti et al., NONCONVENTIONAL ULTRASONOGRAPHY (POWER SPECTRUM ANALYSIS) IN THE MANAGEMENT OF RETINOBLASTOMA, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 69-74

Authors: AMEMIYA T TAKANO J CHOSHI K
Citation: T. Amemiya et al., DID ATOMIC-BOMB RADIATION INFLUENCE THE INCIDENCE OF RETINOBLASTOMA IN NAGASAKI AND HIROSHIMA, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 75-79

Authors: ASSAF AA TABBARA KF ELHAZMI MA
Citation: Aa. Assaf et al., CATARACTS IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 81-86

Authors: OLSEN H BAGGESEN K SJOLIE AK
Citation: H. Olsen et al., CATARACTS IN MORQUIO-SYNDROME (MUCOPOLYSACCHARIDOSIS-IV-A), Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 87-89

Authors: IZQUIERDO NJ MAUMENEE IH TRABOULSI EI
Citation: Nj. Izquierdo et al., ANTERIOR SEGMENT MALFORMATIONS IN 18Q-(DEGROUCHY) SYNDROME, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 91-94

Authors: PINCKERS A CRUYSBERG JRM KREMER H AANDEKERK AL
Citation: A. Pinckers et al., ACETAZOLAMIDE IN DOMINANT CYSTOID MACULAR DYSTROPHY - A PILOT-STUDY, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 95-99

Authors: POTAMITIS T FIELDER AR
Citation: T. Potamitis et Ar. Fielder, ANGLE-CLOSURE GLAUCOMA IN ALAGILLE SYNDROME - A CASE-REPORT, Ophthalmic paediatrics and genetics, 14(2), 1993, pp. 101-104

Authors: REDMOND RM VAUGHAN JI JAY M JAY B
Citation: Rm. Redmond et al., INUTERO DIAGNOSIS OF NORRIE DISEASE BY ULTRASONOGRAPHY, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 1-3

Authors: DOTTI MT BARDELLI AM DESTEFANO N FEDERICO A MALANDRINI A VANNI M GUAZZI GC
Citation: Mt. Dotti et al., OPTIC ATROPHY IN MARINESCO-SJOGREN SYNDROME - AN ADDITIONAL OCULAR FEATURE - REPORT OF 3 CASES IN 2 FAMILIES, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 5-7

Authors: SALVI F SALVI G VOLPE R MENCUCCI R PLASMATI R MICHELUCCI R GOBBI P SANTANGELO M FERLINI A FORABOSCO A TASSINARI CA
Citation: F. Salvi et al., TRANSTHYRETIN-RELATED TTR HEREDITARY AMYLOIDOSIS OF THE VITREOUS BODY- CLINICAL AND MOLECULAR CHARACTERIZATION IN 2 ITALIAN FAMILIES, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 9-16

Authors: DONAHUE SP WENGER SL STEELE MW GORIN MB
Citation: Sp. Donahue et al., BROAD-SPECTRUM MOBIUS SYNDROME ASSOCIATED WITH A 1-11 CHROMOSOME-TRANSLOCATION, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 17-21

Authors: YOUNG WO SMALL KW
Citation: Wo. Young et Kw. Small, PIGMENTED PARAVENOUS RETINOCHOROIDAL ATROPHY (PPRCA) WITH OPTIC DISC DRUSEN, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 23-27
Risultati: 1-25 | 26-29