A. Habel

发表

Cerebrospinal fluid acid-base status and lactate and pyruvate concentrations after convulsions of varied duration and aetiology in children.

H. Simpson, A. Habel, E. George, 1977, Archives of disease in childhood.

Cerebrospinal fluid acid-base status and lactate and pyruvate concentrations after short (less than 30 minutes) first febrile convulsions in children.

H. Simpson, A. Habel, E. George, 1977, Archives of disease in childhood.

Choice of feeding preparations for the newborn

A. Habel, 1986, Archives of disease in childhood.

Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.

J. Hurst, S. Malcolm, E. Young, 1992, American journal of medical genetics.

Practical guidelines for managing patients with 22q11.2 deletion syndrome.

K. Devriendt, K. Sullivan, A. Bassett, 2011, The Journal of pediatrics.

Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times

H. Firth, A. Gennery, A. Holland, 2014, European Journal of Pediatrics.

Ranitidine in the newborn.

N. Murray, A. Habel, 1988, Archives of disease in childhood.

Premature Rupture of Membranes and Effects of Prophylactic Antibodies

W. Mccrae, A. Habel, N. Conn, 1972 .

Premature rupture of membranes and effects of prophylactic antibiotics.

W. Mccrae, A. Habel, N. Conn, 1972, Archives of disease in childhood.

Dexamethasone in herpes-simplex encephalitis.

J. K. Brown, A. Habel, 1972, Lancet.

Osmolar relation between cerebrospinal fluid and serum in hyperosmolar hypernatraemic dehydration.

H. Simpson, A. Habel, 1976, Archives of disease in childhood.

Fluid and electrolyte metabolism in the newborn infant.

A. Habel, W. Uttley, 1976, Clinics in endocrinology and metabolism.

A case of interstitial deletion of 10q25.2----q26.1.

D. Coleman, D. E. Rooney, A. Habel, 1989, Journal of medical genetics.

Management of cleft lip and palate.

D. Sell, M. Mars, A. Habel, 1996, Archives of disease in childhood.

Management of Cleft Lip and Palate in the Developing World

D. Sell, M. Mars, A. Habel, 2008 .

Syndrome‐specific growth charts for 22q11.2 deletion syndrome in Caucasian children

E. Zackai, D. McDonald-McGinn, N. Unanue, 2012, American journal of medical genetics. Part A.

Core neuropsychological characteristics of children and adolescents with 22q11.2 deletion.

F. Kane, E. Kravariti, Elias Tsakanikos, 2010, Journal of intellectual disability research : JIDR.

Memory in intellectually matched groups of young participants with 22q11.2 deletion syndrome and those with schizophrenia.

R. Murray, S. Frangou, E. Kravariti, 2010, Research in developmental disabilities.

Aids to paediatrics

A. Habel, 1982 .

The Nature of Feeding in Infants with Unrepaired Cleft Lip and/or Palate Compared with Healthy Noncleft Infants

D. Sell, M. Mars, B. Sommerlad, 2007, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Toxic Encephalopathy and Acute Brain‐swelling in Children

A. Habel, J. K. Brown, J. Brown, 1975, Developmental medicine and child neurology.

Proceedings: Osmolar relation between CSF and serum in hyperosmolar hypernatraemic dehydration.

H. Simpson, A. Habel, 1975, Archives of Disease in Childhood.

Rese Mam afte Laure Balara Abst Intro The increa the in ated t the U The has in up to now

C. Quesenberry, A. Capra, M. Puligandla, 2010 .

Acute Respiratory Failure in Bronchiolitis and Pneumonia in Infancy. Modes of Presentation and Treatment

D. Matthew, H. Simpson, A. Habel, 1974, British medical journal.

PATHOGENESIS OF NEONATAL APNOEA

A. Habel, 1977, Developmental medicine and child neurology.

Practical guidelines for managing patients with 22q11.2 deletion syndrome.

K. Devriendt, K. Sullivan, A. Bassett, 2011, The Journal of pediatrics.

Delayed detection of cleft palate: an audit of newborn examination

B. Sommerlad, A. Habel, Joanne Powell, 2005, Archives of Disease in Childhood.

Core neuropsychological characteristics of children and adolescents with 22q11.2 deletion.

F. Kane, E. Kravariti, Elias Tsakanikos, 2010, Journal of intellectual disability research : JIDR.

MUCOPOLYSACCHARIDOSIS-II (HUNTER DISEASE) IN A FEMALE TWIN

S. Malcolm, E. Young, B. Winchester, 1990 .

Symptomatic disorders of cardiac conduction in childhood leukemia.

A. Habel, 1974, American journal of diseases of children.