I. Jeffrey

发表

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

D. Kullmann, E. Behr, S. Sisodiya, 2018, The Lancet.

Sites of recurrent tumour after ‘curative’ colorectal surgery: Implications for adjuvant therapy

J. Gilbert, A. Kark, I. Jeffrey, 1984, The British journal of surgery.

A newly recognized autosomal recessive syndrome with abnormal vertebral ossification, rib abnormalities, and nephrogenic rests

F. Prefumo, B. Thilaganathan, T. Homfray, 2003, American journal of medical genetics. Part A.

Prognostic value of tumour thickness in cutaneous malignant melanoma

P. Royston, G. Slavin, C. Sowter, 1983, Journal of clinical pathology.

Stillbirth and intrauterine fetal death: role of routine histopathological placental findings to determine cause of death

M. Ashworth, N. Sebire, J. Hutchinson, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Stillbirth and intrauterine fetal death: contemporary demographic features of >1000 cases from an urban population

M. Ashworth, N. Sebire, I. Jeffrey, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype

S. Bewley, R. Nash, A. Offiah, 2003, Journal of medical genetics.

Biallelic mutations in NRROS cause an early onset lethal microgliopathy

M. Nolan, B. McColl, Y. Crow, 2020, Acta Neuropathologica.

overlapping phenotype punctata (CDPX2): presentation of two cases with dominant Conradi-Hünermann chondrodysplasia Greenberg dysplasia (HEM) and lethal X linked

S. Bewley, R. Nash, A. Offiah, 2006 .

The critical role of perinatal pathology

I. Jeffrey, 2003, BJOG : an international journal of obstetrics and gynaecology.

Polycystin expression during embryonic development of human kidney in adult tissues and ADPKD tissue

B. Weston, R. G. Price, S. Jeffery, 1997, The Histochemical Journal.

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

M. Pourfarzam, J. Zschocke, S. Kölker, 2003, Neuropediatrics.

Osteoclast-type giant cell tumour of the pancreas.

B. Ellis, I. Jeffrey, J. Crow, 1983, Journal of clinical pathology.

Bilateral communicating bronchopulmonary foregut malformations in an infant with multiple congenital anomalies

R. Given-Wilson, M. Murray, I. Jeffrey, 2005, Pediatric Radiology.

Prenatal diagnosis of segmental spinal dysgenesis

B. Thilaganathan, P. Rich, A. Papageorghiou, 2007, Prenatal diagnosis.

Clinical features of molecular pathology of solid tumours in childhood.

R. Nash, K. Pritchard-Jones, B. Messahel, 2005, The Lancet. Oncology.

Color Atlas of Gross Placental Pathology

I. Jeffrey, 1995 .

Noncardiac genetic predisposition in sudden infant death syndrome

E. Behr, M. Simpson, D. Tester, 2018, Genetics in Medicine.

The pathology of meconium ileus equivalent.

H. Fox, M. Wells, I. Jeffrey, 1983, Journal of clinical pathology.

Systematic review and meta‐analysis of appendiceal carcinoid tumors in children

I. Jeffrey, C. Sinha, B. Okoye, 2018, Pediatric blood & cancer.

Congenital vascular malformations: A series of five prenatally diagnosed cases

S. Mansour, B. Thilaganathan, T. Homfray, 2008, American journal of medical genetics. Part A.

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

E. Behr, M. Simpson, D. Tester, 2018, Journal of the American College of Cardiology.

Cholelithiasis in a preterm infant.

A. Whitelaw, I. Jeffrey, R. J. Lund, 1984, Pediatric pathology.

Exome‐Wide Rare Variant Analyses in Sudden Infant Death Syndrome

E. Behr, M. Simpson, D. Tester, 2018, The Journal of pediatrics.

Intrapartum Asphyxia and Birth Trauma

I. Jeffrey, 2001 .

Oral Clindamycin and Histologic Chorioamnionitis in Women With Abnormal Vaginal Flora

A. Ugwumadu, I. Manyonda, P. Hay, 2006, Obstetrics and gynecology.

CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non‐immune hydrops fetalis

S. Mansour, G. Brice, V. Murday, 2012, Clinical genetics.

Organ weights and ratios for postmortem identification of fetal growth restriction: utility and confounding factors

M. Ashworth, N. Sebire, J. Hutchinson, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Surgical Pathology Techniques

D. Lowe, I. Jeffrey, 1990 .