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- TEXTBOOK
OF MEDICINE FOR STUDENTS: A.F. Golwalla, XII, XIII & XIV Editions:
EDITOR of section entitled DISEASES OF CHILDREN DISEASES OF CHILDREN.
Author of chapters on (1) Growth and Development (2) Vomiting and Regurgitation
in the Newborn (3) Respiratory Distress in the Newborn and Hyaline Membrane
Disease (4) Infections in the newborn (5) Failure to thrive (6) Indian
Childhood Cirrhosis.
- Savliwala
AS, Naik GG, Bharucha BA, Khare RD, Kumta NB: SANDHOFF DISEASE - GM2
GANGLIOSIDOSIS TYPE 2. Ind. Pediatr. 20(2), 1983, 134-137.
- Bharucha
BA, Agarwal UM, Savliwala AS, Kolluri R, Kumta NB: TRISOMY 18 - EDWARD'S
SYNDROME - A REPORT OF THREE CASES. J. Postgrad. Med. 29 (2), 1983,
129-132.
- Bharucha
BA, Savliwala AS, Koppikar GV, Kumta NB : SIBLINGS WITH LARSEN'S SYNDROME.
Indian Pediatr. 20(5),1983,375-377.
- Bharucha
BA, Savliwala AS, Koppikar GV, Kumta NB : COMPTOMELIC DWARFISM SYNDROME.
J. Postgrad. Med. 29(4),1983,168-170.
- Bharucha
BA, Naik GG, Savliwala AS, Joshi RM, Kumta NB: SIBLINGS WITH THE AUSTIN
VARIANT OF METACHROMATIC LEUKODYSTROPHY - MULTIPLE SULFATIDOSIS. Ind.
J. Pediatr.51,1984,477-480.
- Bharucha
BA, Savliwala AS, Koppikar GV, Naik GG, Kumta NB: AN APPROACH TO DIAGNOSIS
OF THE HEPATIC GLYCOGENOSES. Ind. Pediatr. 21(11),1984, 855-863.
- Joshi
RM, Bharucha BA, Patwardhan SD, Kumta NB: HEMANGIOMATOUS MALFORMATION
OF THE THORACIC VERTEBRA. Ind. Pediatr. 21(11), 1984, 900-903.
- Joshi
RM, Bharucha BA, Kumta NB: CONGENITAL LIMB DEFECTS. Ind. Pediatr. 22(2),1985,107-112.
- Khanna
SS, Bharucha BA, Bhatia AK, Dastur FD: NEONATAL TETANUS- PSYCHOMOTOR
DEVELOPMENT IN SURVIVORS. Ind. Pediatr.22 (2), 1985, 125-130.
- Joshi
RM, Mohire MD, Bharucha BA, Kumta NB: POMPE'S DISEASE. Ind. Pediatr.
22(4),1985,315-318.
- Joshi
RM, Bharucha BA, Kumta NB, Vengsarkar AS: LIMB HEART SYNDROMES Ind.
Pediatr. 22(5), 1985,355-359.
- Joshi
RM, Bharucha BA, Mohire MD, Kumta NB: CONGENITAL MYAESTHENIA GRAVIS.
J Postgrad. Med. 31(2) 1985,109-111.
- Koppikar
GV, Joshi RM, Bharucha BA, Kumta NB: CRANIOFACIAL MALFORMATIONS. Ind.
Pediatr. 22(6), 1985, 411-414.
- Joshi
RM, Bharucha BA, Kumta NB, Ramakantan R: THE GENETICS OF CONGENITAL
DWARFISM. Ind. J. Pediatr. 52, 1985, 545-547.
- Pandya
AL, Bharucha BA, Patwardhan SD, Kagalwalla TY, Kumta NB: A MULTIPLE
MALFORMATION SYNDROME WITH CLEFT LIP AND PALATE AND ANKYLOBLEPHARON
FILIFORM ADNATUM. Ind. J. Pediatr. 52, 1985,667-670.
- Kumta
NB, Bharucha BA, Pandya Al, Kagalwalla TY, Vaidya VU, Rane SM : MENKES
STEELY HAIR DISEASE. Ind. Pediatr. 23 (1), 1986, 64-67.
- Joshi
RM, Bharucha BA, Ramakantan R, Kumta NB: AN OVERVIEW OF CONGENITAL MALFORMATIONS
OF THE RESPIRATORY TRACT. Ind. J. Chest Dis. & All. Sciences. 28
(1), 1986, 6-10.
- Bharucha
BA, Kagalwalla TY, Pandya AL, Vaidya VU, Kumta NB: CYPROHEPTADINE POISONING.
Ind. Pediatr. 24 (2), 1987, 165-169.
- Bharucha
BA et al: CYPROHEPTADINE POISONING. Abstract in Toxicology Abstracts,
Cambridge Scientific Abstracts, 10(7),1987, 19.
- Joshi
RM, Pandya AL, Bharucha BA, Ramakantan R, Kumta NB: ACRODYSOSTOSIS SYNDROME.
Ind. J. Pediatr. 54, 1987,271-273.
- Kagalwalla
TY, Vaidya VU, Bharucha BA, Pandya AL, Kumta NB: CAVERNOUS HEMANGIOMAS
OF THE LIVER AND SPLEEN. Ind. Pediatr.24 (5),1987,427-430.
- Vaidya
VU, Sidhwa SJ, Bharucha BA, Kagalwalla TY, Kumta NB: MURCS ASSOCIATION
Ind. Pediatr.24 (7),1987,588-592.
- Joshi
RM, Kagalwalla TY, Bharucha BA, Vaidya VU, Pandya AL, Parikh AP, Kumta
NB: WILSON'S DISEASE - A STUDY OF 12 CASES. Ind. J. Gastroenterol..
6 (4),1987,227-228.
- Vaidya
VU, Bharucha BA, Kagalwalla TY, Pandya AL, Kumta NB:FARBER'SLIPOGRANULOMATOSIS.
Ind.Pediatr.24(8),1987, 673-675.
- Kagalwalla
TY, Vaidya VU, Joshi RM, Bharucha BA, Kumta NB: CHONDROECTODERMAL DYSPLASIA.
Ind. Pediatr. 24 (11),1987, 1045-1050.
- Sardharwalla
IB, Lingam S, Herrey DR: PREVENTION OF MENTAL HANDICAP IN DEVELOPING
COUNTRIES Arch. Dis. Child. 61, 1986, 411-412. (Acknowledgements to
NB Kumta & BA Bharucha)
- Vaidya
VU, Parikh AP, Bharucha BA, Kumta NB: LANGER GIEDION SYNDROME. Ind.
Pediatr. 25 (1), 1988, 99-101.
- Parikh
AP, Bharucha BA, Kumta NB:CAUDAL REGRESSION SYNDROME. Ind. Pediatr.
25 (3), 1988, 299-302.
- Parikh
AP, Khubchandani RP, Bharucha BA, Kumta NB, Pandya MB, Naik GG: ALKAPTONURIA
- A SERIES OF SEVEN CASES J. Assoc. Physicians India 36 (9),1988.565-566.
- Sundaram
U, Bharucha BA, Kumta NB, Date U, Kallapur SG: SYNDROME MYXOMA. Ind.
Peditr. 25 (9), 1988,888-891.
- Sundaram
U, Kallapur SG, Kumta NB, Bharucha BA, Shah NF, Borwankar SS: IDIOPATHIC
INTERSTITIAL CALCINOSIS. Ind. Pediatr. 25 (10), 1988,1002-1005.
- Joshi
RM, Bharucha BA, Kumta NB: NEUROCUTANEOUS DISEASES - A STUDY OF 61 CASES.
Ind. J. Pediatr. 55, 1988, 617-626.
- Kagalwalla
TY, Bharucha BA, Kumta NB, Naik GG: THE MUCOPOLYSACCHARIDOSES - A STUDY
OF 48 CASES. Ind J. Pediatr.55, 1988, 919-925.
- Kagalwalla
TY, Bharucha BA, Khare RD, Kumta NB: DIAGNOSTIC APPROACH TO COARSE FACIES
Ind. J. Pediatr. 55,1988,861-870.
- Kagalwalla
TY, Kallapur SG, Rathore AS, Bharucha BA, Irani SF, Sane SY, Parikh
DA:CONGENITAL HISTIOCYTOSIS- X Ind. Pediatr. 26 (3), 1989, 292-296.
- Parikh
AP, Vaidya VU, Bharucha BA, Kumta NB: PACHYONYCHIA CONGENITA - A CASE
REPORT. J. Postgrad. Med. 35 (3), 1989, 189.
- Khubchandani
RP, Parikh AP, Vaidya VU, Bharucha BA, Kumta NB:UNUSUAL BONE CHANGES
IN CONGENITAL SYPHILIS Ind. Pediatr. 26 (6), 1989. 603-607.
- Lohe AS,
Bharucha BA: PROTEIN ENERGY MALNUTRITION PART I - (SPECIAL ARTICLE FOR
LAY PRESS) : 2001 (Times of India group of publications), April1989,
58-62.
- Lohe AS,
Bharucha BA: PROTEIN ENERGY MALNUTRITION PART II - (SPECIAL ARTICLE
FOR LAY PRESS) : 2001 (Times of India group of publications), May 1989,
58-64.
- Bharucha
BA: EARLY DIAGNOSIS OF CEREBRAL PALSY (SPECIAL Article). Pediatr. Clin.
India. Vol.25 No. 1, 1990.
- Deshpande
PG, Wagle SU, Mehta SD, Bharucha BA, Irani SF: NEONATAL OSTEOMYELITIS
AND SEPTIC ARTHRITIS Ind. Pediatr. 27 (5), 1990, 453-457.
- Bhatawadekar
AM, Kumta NB, Dave KH, Bharucha BA: EFFICACY OF THREE DOSES OF ORAL
POLIO IMMUNISATION BEGINNING WITHIN THE FIRST FOUR DAYS OF LIFE Ind.
Pediatr. 27 (9),1990, 911-917.
- Bharucha
BA, Khubchandani RP, Vaidya PV, Kher AS, Kumta NB: PROTEUS SYNDROME
Ind Pediatr. 27(12),1990,1312-1316.
- TEXTBOOK
ON "THE ADOLESCENT GIRL"- Krishna, Parulekar, Salvi (Eds.),1991.
Chapters on (1) "GENETIC DISORDERS OF THE ADOLESCENT GIRL"
, (2)INTERSEX.
- Dutta
S, Bharucha BA, Vaidya PV, Kher AS, Kumta NB: 20 p deletion SYNDROME
- REPORT OF A CASE WITH UNUSUAL SKELETAL FEATURES Ind. J. Pediatr. 58
(5),701,1991.
- Kher AS.,
Bharucha BA, Kumta NB: WILSON'S DISEASE - INITIAL WORSENING OF THE NEUROLOGICAL
SYNDROME WITH PENICILLAMINE THERAPY - Ind. Pediatr. 29(7),1992, pp 927-929.
- John B,
Chakrapani A, Sanklecha MU, Kher AS, Bharucha BA, Kumta NB; MELKERSSON
ROSENTHAL SYNDROME, OLIGOSYMTOMATIC FORM. Ind. Pediatr. 29(9),1992,
pp 1163-1165.
- Wadhwa
N, Bharucha BA, Chablani U, Contractor N: AN EPIDEMIOLOGICAL STUDY OF
FEBRILE SEIZURES IN CHILDHOOD WITH SPECIAL REFERENCE TO FAMILY HISTORY
AND HLA LINKAGE. Ind. Pediatr. 29(12),1992, pp 1479-1485.
- Mahajan
M, Kher AS, Khungar A, Bhat M, Sanklecha MU, Bharucha BA: MURCS ASSOCIATION
- A REVIEW OF 7 CASES. J. Postgrad, Med. 38(3),1992, pp 109-110.
- Sanklecha
MU, Kher AS, Bharucha BA - ASYMMETRIC CRYING FACIES: THE CARDIOFACIAL
SYNDROME - J. Postgrad Med. 38(3),1992, pp 147-148.
- Gupte
G, Mahajan P, Shreeniwas VK, Kher AS, Bharucha BA: WILDERVANCK SYNDROME
(CERVICO-OCULO-ACOUSTIC SYNDROME): J. Postgrad Med. 38(4),1992, pp.
181-182.
- Kher AS,
Bharucha BA, Kamat JR, Kurkure P: CYSTIC TUBERCULOSIS OF BONES. Ind.
Pediatr. 30(5),1993, pp 676-678.
- Alavi
Said, Kher AS, Kumar A, Muranjan M, Bharucha BA: COHEN SYNDROME. Ind.
Pediatr. 30(5),1993, pp. 678-681.
- Parikh
S, Bharucha BA, Kamdar S, Kshirsagar N: POLYMORPHONUCLEAR LEUKOCYTE
FUNCTIONS IN CHILDREN WITH CYANOTIC AND ACYANOTIC CONGENITAL HEART DISEASE:
Ind. Pediatr. 30(7),1993, pp. 883-890.
- Udwadia
AD, Chattopadhyay A, Bharucha BA, Kher A. TRILOBED SKULL. RADIOLOGICAL
CASE OF THE MONTH. J Applied Med 1993;19(10):779-781.
- Alavi
Said, Chakrapani A, Kher AS, Bharucha BA: PROTEUS SYNDROME. J. Postgrad.
Med. 1993;39(4):219-221.
- Chattopadhyay
A, Kher AS, Udwadia AD, Sharma SV, Bharucha BA, Nicholson A.: FRASER
SYNDROME. J. Postgrad. Med. 1993;39(4):226-230.
- Kher A,
Bhat M, Ratnam KL, Khambadkone S, Bharucha BA, Irani SF : SPONDYLOCOSTAL
DYOSTOSIS. Indian J. Pediatr, 1993,60:813-818.
- Bawa HS,
Kher A, Doraiswamy A, Malik AK, Bharucha BA, Kamat JR : MASSIVE HEMOPTYSIS
CONTROLLED BY BRONCHIAL ARTERY EMBOLISATION : A CASE REPORT. Ind. J.
Chest Dis. Allied Sci., 36;1:1994,31-34.
- Gupte
GL, Kher AS, Kanade SP, Bharucha BA, Sagade SN : ACRODYSOSTOSIS WITH
5 ALPHA REDUCTASE DEFICIENCY : AN UNUSUAL ASSOCIATION. Ind. J. Pediatr,
1994;61:287-306.
- Sanklecha
MV, Kher A, Naik CG, Bharucha BA, Mahajan P : STORAGE DISORDERS PRESENTING
LIKE MUCOPOLYSACCHARIDOSIS. Indian J. Pediatr, 1994;61:367-372.
- Shreeniwas,
Kher A, Datta S, Kanade S, Vaidya M, Bharucha BA : MIXED GONADAL DYSGENESIS
WITH 45X/46XX/46XY MOSAICISM. Letter, Indian J. Pediatr, 1994;61:445-446.
- Alavi
S, Kher A, Bharucha BA : SCHINZEL GIDIEON SYNDROME. Indian Pediatr,
1994;31(a):1111-1114.
- Mahajan
PV, Bharucha BA. : EVALUATION OF SHORT NECK : NEW NECK LENGTH PERCENTILES
AND LINEAR CORRELATIONS WITH HEIGHT AND SITTING HEIGHT. Indian Pediatr,
1994;31(10):1193-1203.
- Doraiswamy
A, Iyer S, Kher AS, Bharucha BA. DIASTROPHIC DYSPLASIA. Indian Pediatr,
1994;31(11):1403-1405.
- Chattopadhyay
A, Shah AM, Khambadkone SM, Dixit KM, Bharucha BA, Irani SF. JOUBERT
SYNDROME. Indian Pediatr, 1994,31(11):1415-1418.
- Kher A,
Chattopadhyay A, Khambekar K, Divekar A, Bharucha BA. JOUBERTS SYNDROME
WITH POLYDACTYLY AND OPTIC COLOBOMA IN 2 SIBS. Ind J Pediatr, 1994;61(6):729-732.
- Kher AS,
Chattopadhyay A, Datta S, Kanade S, Sreenivasan VK, Bharucha BA. FAMILIAL
MOSAIC TURNER SYNDROME. Clin Genet. 1994;46(5):382-383.
- Chattopadhyay
A, Kher AS, Thamke RH, Deshmukh CT, Bharucha BA. NEUROFIBROMATOSIS PRESENTING
WITH ACQUEDUCTAL STENOSIS. Indian J. Pediatr, 1994;61:586-587.
- Bharucha
BA, Kher A (eds.). GENETIC DISORDERS IN CHILDREN. Part 1. Pediatr Clinics
India 1993,28(3).
- Bharucha
BA, Kher A (eds.). GENETIC DISORDERS IN CHILDREN. Part 2. Pediatr Clinics
India, 1995.
- Gupte
GL, Kher AS, Joshi SM, Bharucha BA, Kanade SP. LISSENCEPHALY. Indian
Pediatr, 1995,32(5),593-596.
- Malhotra
NJ, Kher A, Uthup S, Mohan PV, Bharucha BA, Pathre AV. IDIOPATHIC PULMONARY
HEMOSIDEROSIS. Indian J Chest Dis Allied Sci, 37,3, 1995;pp 175-178.
- Gupte
GL, Kher AS, Bansal S, Bharucha BA, Kanade SP, Sharma SV. IF THE IRIS
IS ABSENT? Letter. Indian Pediatr 1995,32(6),702-703.
- Gupte
GL, Kotvaliwale SV, Mahajan PV, Kher AS, Kanade SP, Bharucha BA. 48
XXXY VARIANT OF KLINEFELTER SYNDROME. Indian Pediatr, 1995,32(7),798-801.
MICROCORNEA GLAUCOMA AND ABSENT FRONTAL SINUS. Letter J Pediatr 1995;127(2):333.
- Gupte
GL, Deshmukh CT, Bharucha BA, Irani SF. KLIPPEL-TRENAUNAY-WEBER SYNDROME
WITH HYDROCEPHALUS : AN UNUSUAL ASSOCIATION. Pediatr Neurosurgery, 1995,22:328-329.
- Lalwani
S, Kher AS, Shridhar N, Naik GG. MUCOLIPIDOSIS II, A REPORT OF 3 CASES.
Ind. J. Pediatr 1995,62,120-123.
- Bharucha
BA, Kher AS. GENETICS IN ORTHOPAEDICS - Chapter in Textbook of Orthopaedics
for developing countries. Johari A.N. (ed.). In press.
- Bharucha
BA. PRENATAL DIAGNOSIS OF GENETIC DISORDERS. Chapter in Recent Advances
in Pediatrics. Vol.6, Gupte S. (ed.). p 1-30.
API Textbook of Medicine 6th Edition, 3 Chapters on (i) Gene Tracking
and Mapping - Theoretical Principles (ii) DNA analysis & isolation
of genes - laboratory techniques (iii) Gene therapy. Sainani GS, Dastur
FD (eds.)
- Monograph
on Adolescent Gynaecology; Orient Longman, Chapter on "Intersex
- Genetic Aspects".
- Shah AM,
Chattopadhyay A, Kher A, Bharucha BA, Karapurkar AP. CRANIOSYNOSTOSIS
WITH MARFAN SYNDROME, HAND AND FOOT ANOMALIES. Letter; Clinical Dysmorphology1996;5:263-266.
- Udwadia
AD, Khambadkone S, Bharucha BA, Lokhandwala Y, Irani SF. FAMILIAL CONGENITAL
VALVAR PULMONARY STENOSIS : AUTOSOMAL DOMINANT INHERITANCE. Pediatr
Cardiol 1996;17:407-409.
- Chattopadhyay
A, Shah AM, Kher A, Bharucha BA, Karapurkar AP. CRANIOSYNOSTOSIS AND
KLIPPEL FEIL SYNDROME : A NEW ASSOCIATION. Indian J Pediatr, 1996;63:819-822.
- Kaur M,
Kabra M, Kher AS, Naik GG, Bharucha BA. Verma IC: CLINICAL AND ENZYME
STUDIES IN GAUCHER DISEASE Ind. Pediatr.1996,33(9),735-738.
- Kher A,
Gahankari DR, Tambwekar SR, Doraiswamy A, Iyer S, Bharucha BA, Rana
RE. SUPERNUMERARY LIMBS - A CASE REPORT OF A RARE CONGENITAL ANOMALY.
Annals of Plastic Surgery,1996,37(5),549-552.
- Bharucha
BA, Kher A. SPECTRUM OF INHERITED METABOLIC DISEASE IN INDIA - A 17
YEAR EXPERIENCE. Sent for publication to J Hum Genetics.
- Iyer SL,
Duraiswamy A, Kher AS, Joshi S, Bharucha BA, Kanade S. Cri du chat syndrome.
J Postgrad Med. 1996 Jul-Sep;42(3):86-8.
- Tullu
MS, Muranjan MN, Sharma SV, Sahu DR, Swami SR, Deshmukh CT, Bharucha
BA. Cri-du-chat syndrome: clinical profile and prenatal diagnosis. J
Postgrad Med. 1998 Oct-Dec;44(4):101-4.
- Muranjan
MN, Bharucha BA, Kirtane MV, Deshmukh CT. Mondini dysplasia of the inner
ear with CSF leak-A rare cause of recurrent meningitis. Indian Pediatr.
1999 Apr;36(4):401-6.
- Tullu
MS, Arora P, Deshmukh CT, Muranjan MN, Bharucha BA. Benzathine penicillin
induced immune haemolytic anaemia. J Postgrad Med. 1999 Apr-Jun;45(2):58-9.
- Tullu
MS, Deshmukh CT, Save SU, Bhoite BK, Bharucha BA. Superior sagittal
sinus thrombosis: a rare complication of nephrotic syndrome. J Postgrad
Med. 1999 Oct-Dec;45(4):120-2.
- Surve
TY, Muranjan MN, Deshmukh CT, Warke CS, Bharucha BA. Inflammatory linear
verrucous epidermal nevus syndrome with bilateral vertebral artery occlusion.
Indian Pediatr. 1999 Aug;36(8):820-3.
- Tullu
MS, Deshmukh CT, Vaideeswar P, Bharucha BA, Arora PK. Mediastinal yolk
sac tumor--a rare presentation. Indian Pediatr. 1999 Dec;36(12):1259-62.
- Tullu
MS, Muranjan MN, Save SU, Deshmukh CT, Khubchandani SR, Bharucha BA.
Dorfman-Chanarin syndrome: a rare neutral lipid storage disease. Indian
Pediatr. 2000 Jan;37(1):88-93.
- Muranjan
MN, Gurav M, Surve T, Deshmukh CT, Bharucha BA. Familial glucocorticoid
deficiency, alacrimia and achalasia--Allgrove syndrome. Indian J Pediatr.
1999 Jan-Feb;66(1):151-4.
- Mishra
P, Muranjan M, Bharucha BA. Autosomal dominant ectrodactyly with sensorineural
deafness. Clin Dysmorphol. 2000 Apr;9(2):119-21.
- Muranjan
MN, Bharucha BA. Unusual hand malformations with cardiac defects--a
variant of heart--hand syndrome IV. Indian J Pediatr. 2000 May;67(5):392-4.
- Tullu
MS, Muranjan MN, Kondurkar PP, Bharucha BA. Krabbe disease--clinical
profile. Indian Pediatr. 2000 Sep;37(9):939-46.
- Tullu
MS, Muranjan MN, Kantharia VC, Parmar RC, Sahu DR, Bavdekar SB, Bharucha
BA. Neurofibromatosis-Noonan syndrome or LEOPARD Syndrome? A clinical
dilemma. J Postgrad Med. 2000 Apr-Jun;46(2):98-100.
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